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FDA 510(k)

COMP. CLIN. CHEM. CONTROL SERUM-DECISION

K-Number: K780552 · 1978-05-19

ApplicantBeckman Instruments, Inc.
Decision Date1978-05-19
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COMP. CLIN. CHEM. CONTROL SERUM-DECISION 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 1978-05-19 under 510(k) number K780552. 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 COMP. CLIN. CHEM. CONTROL SERUM-DECISION?

COMP. CLIN. CHEM. CONTROL SERUM-DECISION is a medical device that received FDA 510(k) clearance on 1978-05-19. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K780552.

When did COMP. CLIN. CHEM. CONTROL SERUM-DECISION receive FDA 510(k) clearance?

COMP. CLIN. CHEM. CONTROL SERUM-DECISION received FDA 510(k) clearance on 1978-05-19, under 510(k) number K780552.

Who is the listed applicant for COMP. CLIN. CHEM. CONTROL SERUM-DECISION?

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 COMP. CLIN. CHEM. CONTROL SERUM-DECISION?

The FDA product code for COMP. CLIN. CHEM. CONTROL SERUM-DECISION is JJY.

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Other records listing Beckman Instruments, Inc. as applicant

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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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