LACIMAL INTUBATION SETS— 510(k) K831901

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K831901 for LACIMAL INTUBATION SETS, Substantially Equivalent on 1983-07-12. Applicant: Visitec Co.. Device class: 1.

Clearance details

Applicant: Visitec Co.
Product code: Code HNL
Device class: Class 1
Regulation: 21 CFR 886.4350
Advisory panel: Ophthalmic
Date received: 1983-06-14
Decision date: 1983-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code HNL

K843491 — CONCEPT FIBER OPTIC CANALICULUS INTUBA1984-10-05
K840861 — TSE-ANDERSON MODIFIED LACRIMAL GROOV1984-05-09
K833671 — STERILE OIL AND GUIDEWIRE1984-01-10
K813187 — PILLING LACRIMAL INTUBATION SYSTEM1982-01-28
K812255 — ETHICON LACRIMAL STENT1981-08-20

More clearances from Visitec Co.

K953394 — VISITEC COLLAR BUTTON CATHETER {GRIFFITHS}1995-10-12
K945114 — VISITEC SCLERAL PLUG1995-02-23
K945738 — VISIFLEX OPHTHALMIC SURGICAL INCISE DRAPE1995-02-14
K945172 — VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS1995-01-17
K942234 — VISITEC PRECISE-POINT1994-07-12

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