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FDA 510(k)

RELIANCE TEMPO OPHTH. INSTR STAND

K-Number: K831568 · 1983-06-30

Decision Date1983-06-30
Product CodeHHF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

RELIANCE TEMPO OPHTH. INSTR STAND 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 1983-06-30 under 510(k) number K831568. The device is classified under product code HHF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIANCE TEMPO OPHTH. INSTR STAND?

RELIANCE TEMPO OPHTH. INSTR STAND is a medical device that received FDA 510(k) clearance on 1983-06-30. The listed applicant is F. & F. Koenigkramer. The 510(k) number is K831568.

When did RELIANCE TEMPO OPHTH. INSTR STAND receive FDA 510(k) clearance?

RELIANCE TEMPO OPHTH. INSTR STAND received FDA 510(k) clearance on 1983-06-30, under 510(k) number K831568.

Who is the listed applicant for RELIANCE TEMPO OPHTH. INSTR STAND?

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 TEMPO OPHTH. INSTR STAND?

The FDA product code for RELIANCE TEMPO OPHTH. INSTR STAND is HHF.

Related Clinical Trials

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.

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.

View all 9 devices →

Related Devices (Code: HHF)

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.

Official Source

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

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