RELIANCE OPHTHALMIC INSTRUMENT CONTROL— 510(k) K812544

Name: FDA 510(k) clearance K812544
Creator: U.S. Food and Drug Administration
Published: 1981-09-21

Substantially Equivalent

F. & F. Koenigkramer

FDA 510(k) clearance K812544 for RELIANCE OPHTHALMIC INSTRUMENT CONTROL, Substantially Equivalent on 1981-09-21. Applicant: F. & F. Koenigkramer. Device class: 1.

Clearance details

Applicant: F. & F. Koenigkramer
Product code: Code HMF
Device class: Class 1
Regulation: 21 CFR 886.1860
Advisory panel: Ophthalmic
Date received: 1981-09-04
Decision date: 1981-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K935945 — ROTA DATAMATE I1994-04-19
K935952 — ROTA SYSTEM 50001994-04-19
K931839 — ROTA SYSTEM XL1993-11-22
K930440 — MARCO INTERNATIONAL STAND1993-07-06
K924771 — BURTON OPHTHALMIC STAND - MODEL XL32001993-04-05

More clearances from F. & F. Koenigkramer

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K860519 — RELIANCE MODEL 200 PODIATRY CHAIR1986-02-19
K853149 — RELIANCE 1000, RELIANCE 1500, RELIANCE 20001985-09-05
K853150 — RELIANCE 61001985-09-05
K853151 — RELIANCE 50001985-09-05
K843046 — RELIANCE TREATMENT CABINET1984-09-27

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