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FDA 510(k)

RELIANCE OPHTHALMIC INSTRUMENT CONTROL

K-Number: K812544 · 1981-09-21

ApplicantF. & F. Koenigkramer
Decision Date1981-09-21
Product CodeHMF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RELIANCE OPHTHALMIC INSTRUMENT CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is F. & F. Koenigkramer. It received FDA 510(k) clearance on 1981-09-21 under 510(k) number K812544. The device is classified under product code HMF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIANCE OPHTHALMIC INSTRUMENT CONTROL?

RELIANCE OPHTHALMIC INSTRUMENT CONTROL is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is F. & F. Koenigkramer. The 510(k) number is K812544.

When did RELIANCE OPHTHALMIC INSTRUMENT CONTROL receive FDA 510(k) clearance?

RELIANCE OPHTHALMIC INSTRUMENT CONTROL received FDA 510(k) clearance on 1981-09-21, under 510(k) number K812544.

Who is the listed applicant for RELIANCE OPHTHALMIC INSTRUMENT CONTROL?

The FDA 510(k) record lists F. & F. Koenigkramer as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELIANCE OPHTHALMIC INSTRUMENT CONTROL?

The FDA product code for RELIANCE OPHTHALMIC INSTRUMENT CONTROL is HMF.

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Other records listing F. & F. Koenigkramer as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K860519RELIANCE MODEL 200 PODIATRY CHAIRK853151RELIANCE 5000K853150RELIANCE 6100K853149RELIANCE 1000, RELIANCE 1500, RELIANCE 2000K843046RELIANCE TREATMENT CABINETK834060RELIANCE OPHTHALMIC SLIT LAMP R-083

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Related Devices (Code: HMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K935945ROTA DATAMATE IRota Systems,Inc.K935952ROTA SYSTEM 5000Rota Systems Medfurniture, Inc.K931839ROTA SYSTEM XLRota Systems Medfurniture, Inc.K930440MARCO INTERNATIONAL STANDMarco Ophthalmic, Inc.K924771BURTON OPHTHALMIC STAND - MODEL XL3200R.H. Burton Co.K924780BURTON OPHTHALMIC EXAM UNIT - MODEL 2201R.H. Burton Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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