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FDA 510(k)

AFRICAN GREEN MONKEY BLOOD IN ALSERVERS

K-Number: K813513 · 1981-12-31

ApplicantDutchland Laboratories, Inc.
Decision Date1981-12-31
Product CodeLHW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AFRICAN GREEN MONKEY BLOOD IN ALSERVERS 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 1981-12-31 under 510(k) number K813513. The device is classified under product code LHW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AFRICAN GREEN MONKEY BLOOD IN ALSERVERS?

AFRICAN GREEN MONKEY BLOOD IN ALSERVERS is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K813513.

When did AFRICAN GREEN MONKEY BLOOD IN ALSERVERS receive FDA 510(k) clearance?

AFRICAN GREEN MONKEY BLOOD IN ALSERVERS received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813513.

Who is the listed applicant for AFRICAN GREEN MONKEY BLOOD IN ALSERVERS?

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 AFRICAN GREEN MONKEY BLOOD IN ALSERVERS?

The FDA product code for AFRICAN GREEN MONKEY BLOOD IN ALSERVERS is LHW.

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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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