FOCOMETER— 510(k) K944402

Substantially Equivalent

Lacrimedics, Inc.

FDA 510(k) clearance K944402 for FOCOMETER, Substantially Equivalent on 1994-11-22. Applicant: Lacrimedics, Inc.. Device class: 2.

Clearance details

Applicant: Lacrimedics, Inc.
Product code: Code HLJ
Device class: Class 2
Regulation: 21 CFR 886.1570
Advisory panel: Ophthalmic
Date received: 1994-09-12
Decision date: 1994-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rialto, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HLJ

K142486 — HEINE BETA 200, HEINE BETA 200 S, HEINE K 1802015-05-18
K142837 — HEINE SIGMA 250 & HEINE SIGMA 250 M22015-01-29
K131959 — HEINE MINI 3000(R) OPHTHALMOSCOPE2014-03-07
K131961 — HEINE BETA 200(R) OPHTHALMOSCOPE2013-12-04
K131719 — OPHTHALMOSCOPES DIAGNOSTIC INSTRUMENT KITS2013-10-30

More clearances from Lacrimedics, Inc.

K161673 — LacriPro Punctum Plug2016-11-18
K140026 — COLLASYN PLUG FOR THE LACRIMAL EFFICIENCY TEST2014-06-03
K030300 — OPAQUE HERRICK LACRIMAL PLUG2003-05-09
K021831 — OPAQUE HERRICK LACRIMAL PLUG, 0.3MM,0.5MM,0.7MM, MODELS HLP3-OPB,HLP50OPB,HLP7-OPB2002-07-01
K001737 — OPAQUE HERRICK PLUG, 0.3MM; 0.5MM; O.7MM2000-06-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.