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FDA 510(k)

QUANTITATE ENZYME VERIFIER SET

K-Number: K951293 · 1995-04-20

ApplicantBeckman Instruments, Inc.
Decision Date1995-04-20
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

QUANTITATE ENZYME VERIFIER SET 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 1995-04-20 under 510(k) number K951293. The device is classified under product code JJT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUANTITATE ENZYME VERIFIER SET?

QUANTITATE ENZYME VERIFIER SET is a medical device that received FDA 510(k) clearance on 1995-04-20. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K951293.

When did QUANTITATE ENZYME VERIFIER SET receive FDA 510(k) clearance?

QUANTITATE ENZYME VERIFIER SET received FDA 510(k) clearance on 1995-04-20, under 510(k) number K951293.

Who is the listed applicant for QUANTITATE ENZYME VERIFIER SET?

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 QUANTITATE ENZYME VERIFIER SET?

The FDA product code for QUANTITATE ENZYME VERIFIER SET is JJT.

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Related Devices (Code: JJT)

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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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