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FDA 510(k)

ANTISERUM, HUMAN, IGA

K-Number: K790703 · 1979-04-12

ApplicantKent Laboratories, Inc.
Decision Date1979-04-12
Product CodeCZP
Advisory CommitteeIM
DecisionUnknown

Device Summary

ANTISERUM, HUMAN, IGA 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 1979-04-12 under 510(k) number K790703. The device is classified under product code CZP. It was reviewed by the IM advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ANTISERUM, HUMAN, IGA?

ANTISERUM, HUMAN, IGA is a medical device that received FDA 510(k) clearance on 1979-04-12. The listed applicant is Kent Laboratories, Inc.. The 510(k) number is K790703.

When did ANTISERUM, HUMAN, IGA receive FDA 510(k) clearance?

ANTISERUM, HUMAN, IGA received FDA 510(k) clearance on 1979-04-12, under 510(k) number K790703.

Who is the listed applicant for ANTISERUM, HUMAN, IGA?

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, HUMAN, IGA?

The FDA product code for ANTISERUM, HUMAN, IGA is CZP.

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Other records listing Kent Laboratories, Inc. as applicant

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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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