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FDA 510(k)

KERATOME

K-Number: K903912 · 1990-10-17

ApplicantMicro Precision Instrument Co.
Decision Date1990-10-17
Product CodeHNO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KERATOME is the device name listed in this FDA 510(k) record. The listed applicant is Micro Precision Instrument Co.. It received FDA 510(k) clearance on 1990-10-17 under 510(k) number K903912. The device is classified under product code HNO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KERATOME?

KERATOME is a medical device that received FDA 510(k) clearance on 1990-10-17. The listed applicant is Micro Precision Instrument Co.. The 510(k) number is K903912.

When did KERATOME receive FDA 510(k) clearance?

KERATOME received FDA 510(k) clearance on 1990-10-17, under 510(k) number K903912.

Who is the listed applicant for KERATOME?

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

What is the FDA product code for KERATOME?

The FDA product code for KERATOME is HNO.

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Related Devices (Code: HNO)

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.

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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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