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FDA 510(k)

CK ISOENZYME ELECTROPHORESIS CONTROL-I.D

K-Number: K800604 · 1980-04-10

ApplicantBeckman Instruments, Inc.
Decision Date1980-04-10
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CK ISOENZYME ELECTROPHORESIS CONTROL-I.D 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 1980-04-10 under 510(k) number K800604. 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 CK ISOENZYME ELECTROPHORESIS CONTROL-I.D?

CK ISOENZYME ELECTROPHORESIS CONTROL-I.D is a medical device that received FDA 510(k) clearance on 1980-04-10. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K800604.

When did CK ISOENZYME ELECTROPHORESIS CONTROL-I.D receive FDA 510(k) clearance?

CK ISOENZYME ELECTROPHORESIS CONTROL-I.D received FDA 510(k) clearance on 1980-04-10, under 510(k) number K800604.

Who is the listed applicant for CK ISOENZYME ELECTROPHORESIS CONTROL-I.D?

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 CK ISOENZYME ELECTROPHORESIS CONTROL-I.D?

The FDA product code for CK ISOENZYME ELECTROPHORESIS CONTROL-I.D is JJT.

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Other records listing Beckman Instruments, 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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