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FDA 510(k)

GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF

K-Number: K812372 · 1981-09-09

ApplicantDutchland Laboratories, Inc.
Decision Date1981-09-09
Product CodeLHT
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF is the device name listed in this FDA 510(k) record. The listed applicant is Dutchland Laboratories, Inc.. It received FDA 510(k) clearance on 1981-09-09 under 510(k) number K812372. The device is classified under product code LHT. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF?

GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF is a medical device that received FDA 510(k) clearance on 1981-09-09. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K812372.

When did GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF receive FDA 510(k) clearance?

GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF received FDA 510(k) clearance on 1981-09-09, under 510(k) number K812372.

Who is the listed applicant for GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF?

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

What is the FDA product code for GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF?

The FDA product code for GUINEA PIG BLOOD IN ALSEVER'S, CIT., DEF is LHT.

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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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