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FDA 510(k)

ANTISERUM TO HUMAN C-REACTIVE PROTEINS

K-Number: K790716 · 1979-08-03

ApplicantKent Laboratories, Inc.
Decision Date1979-08-03
Product CodeDCN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ANTISERUM TO HUMAN C-REACTIVE PROTEINS 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 1979-08-03 under 510(k) number K790716. The device is classified under product code DCN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTISERUM TO HUMAN C-REACTIVE PROTEINS?

ANTISERUM TO HUMAN C-REACTIVE PROTEINS is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Kent Laboratories, Inc.. The 510(k) number is K790716.

When did ANTISERUM TO HUMAN C-REACTIVE PROTEINS receive FDA 510(k) clearance?

ANTISERUM TO HUMAN C-REACTIVE PROTEINS received FDA 510(k) clearance on 1979-08-03, under 510(k) number K790716.

Who is the listed applicant for ANTISERUM TO HUMAN C-REACTIVE PROTEINS?

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 ANTISERUM TO HUMAN C-REACTIVE PROTEINS?

The FDA product code for ANTISERUM TO HUMAN C-REACTIVE PROTEINS is DCN.

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Other records listing Kent Laboratories, Inc. as applicant

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Related Devices (Code: DCN)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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