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FDA 510(k)

FLUOR. CONJUGATED ANTISERUM

K-Number: K770484 · 1977-03-21

ApplicantKent Laboratories, Inc.
Decision Date1977-03-21
Product CodeDEW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

FLUOR. CONJUGATED ANTISERUM is the device name listed in this FDA 510(k) record. The listed applicant is Kent Laboratories, Inc.. It received FDA 510(k) clearance on 1977-03-21 under 510(k) number K770484. The device is classified under product code DEW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUOR. CONJUGATED ANTISERUM?

FLUOR. CONJUGATED ANTISERUM is a medical device that received FDA 510(k) clearance on 1977-03-21. The listed applicant is Kent Laboratories, Inc.. The 510(k) number is K770484.

When did FLUOR. CONJUGATED ANTISERUM receive FDA 510(k) clearance?

FLUOR. CONJUGATED ANTISERUM received FDA 510(k) clearance on 1977-03-21, under 510(k) number K770484.

Who is the listed applicant for FLUOR. CONJUGATED ANTISERUM?

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

What is the FDA product code for FLUOR. CONJUGATED ANTISERUM?

The FDA product code for FLUOR. CONJUGATED ANTISERUM is DEW.

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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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