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FDA 510(k)

TRYPSIN 1%

K-Number: K771955 · 1977-11-22

ApplicantFlow Laboratories, Inc.
Decision Date1977-11-22
Product CodeIBG
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

TRYPSIN 1% is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1977-11-22 under 510(k) number K771955. The device is classified under product code IBG. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRYPSIN 1%?

TRYPSIN 1% is a medical device that received FDA 510(k) clearance on 1977-11-22. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K771955.

When did TRYPSIN 1% receive FDA 510(k) clearance?

TRYPSIN 1% received FDA 510(k) clearance on 1977-11-22, under 510(k) number K771955.

Who is the listed applicant for TRYPSIN 1%?

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

What is the FDA product code for TRYPSIN 1%?

The FDA product code for TRYPSIN 1% is IBG.

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Other records listing Flow Laboratories, Inc. as applicant

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Related Devices (Code: IBG)

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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