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FDA 510(k)

RESPONSE LIQUID LIGAND ASSAY SERUM

K-Number: K821242 · 1982-05-21

ApplicantBeckman Instruments, Inc.
Decision Date1982-05-21
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RESPONSE LIQUID LIGAND ASSAY SERUM is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1982-05-21 under 510(k) number K821242. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPONSE LIQUID LIGAND ASSAY SERUM?

RESPONSE LIQUID LIGAND ASSAY SERUM is a medical device that received FDA 510(k) clearance on 1982-05-21. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K821242.

When did RESPONSE LIQUID LIGAND ASSAY SERUM receive FDA 510(k) clearance?

RESPONSE LIQUID LIGAND ASSAY SERUM received FDA 510(k) clearance on 1982-05-21, under 510(k) number K821242.

Who is the listed applicant for RESPONSE LIQUID LIGAND ASSAY SERUM?

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

What is the FDA product code for RESPONSE LIQUID LIGAND ASSAY SERUM?

The FDA product code for RESPONSE LIQUID LIGAND ASSAY SERUM is JJY.

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Related Devices (Code: JJY)

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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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