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FDA 510(k)

STEINWAY MICRO-KERATO-TREPHINE

K-Number: K843646 · 1985-01-03

Decision Date1985-01-03
Product CodeHRH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STEINWAY MICRO-KERATO-TREPHINE is the device name listed in this FDA 510(k) record. The listed applicant is Steinway Instrument Co., Inc.. It received FDA 510(k) clearance on 1985-01-03 under 510(k) number K843646. The device is classified under product code HRH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEINWAY MICRO-KERATO-TREPHINE?

STEINWAY MICRO-KERATO-TREPHINE is a medical device that received FDA 510(k) clearance on 1985-01-03. The listed applicant is Steinway Instrument Co., Inc.. The 510(k) number is K843646.

When did STEINWAY MICRO-KERATO-TREPHINE receive FDA 510(k) clearance?

STEINWAY MICRO-KERATO-TREPHINE received FDA 510(k) clearance on 1985-01-03, under 510(k) number K843646.

Who is the listed applicant for STEINWAY MICRO-KERATO-TREPHINE?

The FDA 510(k) record lists Steinway Instrument Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEINWAY MICRO-KERATO-TREPHINE?

The FDA product code for STEINWAY MICRO-KERATO-TREPHINE is HRH.

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.

Related Devices (Code: HRH)

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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