STEINWAY MICRO-KERATO-TREPHINE
K-Number: K843646 · 1985-01-03
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Device Summary
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
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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