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FDA 510(k)

FLUORESCEIN CONJUGATED ANTISERUM

K-Number: K770668 · 1977-04-28

ApplicantKent Laboratories, Inc.
Decision Date1977-04-28
Product CodeDEW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

FLUORESCEIN 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 1977-04-28 under 510(k) number K770668. 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 FLUORESCEIN CONJUGATED ANTISERUM?

FLUORESCEIN CONJUGATED ANTISERUM is a medical device that received FDA 510(k) clearance on 1977-04-28. The listed applicant is Kent Laboratories, Inc.. The 510(k) number is K770668.

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

FLUORESCEIN CONJUGATED ANTISERUM received FDA 510(k) clearance on 1977-04-28, under 510(k) number K770668.

Who is the listed applicant for FLUORESCEIN 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 FLUORESCEIN CONJUGATED ANTISERUM?

The FDA product code for FLUORESCEIN 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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