Product code HQG— Ophthalmic
SUNGLASSES
- Classification name
- Lens, Spectacle, Non-Custom (Prescription)
- Device class
- Class 1
- Regulation
- 21 CFR 886.5844
- Advisory panel
- Ophthalmic
- Total cleared
- 56
- First cleared
- Most recent
Market context for product code HQG
FDA has cleared devices under product code HQG between 1976 and 1994, filed by 48 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
last 15 years- 1994
- 1992
- 1990
- 1988
- 1987
- 1986
- 1985
- 1984
- 1983
- 1982
- 1981
- 1980
- 1979
- 1978
- 1977
Top applicants under product code HQG
Recent clearances under product code HQG
- K935919 — SUNGLASSES
- K920795 — 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX
- K900091 — MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR
- K884360 — SEIKO P-6 PROGRESSIVE SPECTACLE LENSES
- K882814 — NEOLENS PRESCRIPTION SPECTACLE LENS
- K882308 — CR-39 PLASTIC LENSES FOR EYEGLASSES
- K881225 — OPHTHALMIC SPECTACLE LENS BLANKS
- K875063 — SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P.
- K874681 — SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES
- K873245 — AR DIACOAT SINGLE VISION LENSES
- K872506 — MELANITE I
- K871961 — MULTIPLE SPECTACLE LENS
- K865103 — KROM-X LENS SYSTEM
- K863367 — FORMALENS 2000
- K862578 — TECHNA VISION CASTING RESIN
- K861021 — GOTTEX SUNGLASSES
- K861162 — LENS SPECTACLE NON-CUSTOM (PRESCRIPTION)
- K861684 — SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS)
- K861759 — GIRARD SUNGLASSES (NON-PRESCRIPTION)
- K861960 — ZIMLITE LENS
- K860794 — WRAPPERS, SUNGLASSES
- K860955 — SPECTACLES LENS
- K854218 — THE ULTRA-MATE LENS
- K851410 — O.M.S. UV-COLOURS
- K852403 — AURALITE II
- K853110 — SPECTACLE PRESCRIPTION LENSES
- K851163 — SUNGLASES
- K850905 — CR-39 TYPE RESIN
- K844778 — SUNGLASSES
- K842187 — MULTIPLE LENS, SPECTACLES, CUSTOM
- K842189 — MULTIPLE LENS, SPECTACLES CUSTOM
- K844321 — CUSTOM LITE
- K843096 — CRISTY/COTE
- K841248 — SUNGLASSES
- K833259 — MULTIPLE
- K823825 — NOSITE UV INTERIM SPECTACLES
- K822573 — SUNGLASS LENSES
- K821398 — CORNING CPF 550 LENS
- K813130 — SUNGLASSES
- K812441 — DI-CROWN
- K812051 — PHOTOLITE AOLITE TINTOMATIC LENS
- K811554 — BARNES-HIND SPECTACLE LENS CLEANER
- K802651 — POSTOPERATIVE UV GLASSES (PLANO/APHAKIC)
- K802749 — BLENDED BIFOCAL
- K800521 — THE LENS OR OMMI-GARD
- K791901 — BARNES-HIND WETTING & SOAKING SOLUTION
- K791721 — ULTRAVUE BLENDED BIFOCAL LENS
- K790215 — LENS, POLYCORE
- K790251 — FUL-VUE ASPHERIC CATARACT LENS
- K781927 — HUMAN II LENS
- K772221 — LENS, HARD RESIN
- K772124 — LENSES, EYEGLASS, SAFETY
- K772024 — RX LENS SERIES
- K772044 — TECHSIGHT LENSES WITH ZUMA COATING
- K770955 — MIRACLELENS
- K761163 — AD7 PLASTIC MULTIFOCAL EYEGLASS LENS
Data sourced from openFDA. This site is unofficial and independent of the FDA.