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FDA 510(k)

ID ZINE LD ISOENZYME CONTROL ABNORM

K-Number: K843265 · 1984-09-13

ApplicantBeckman Instruments, Inc.
Decision Date1984-09-13
Product CodeJJT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ID ZINE LD ISOENZYME CONTROL ABNORM 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 1984-09-13 under 510(k) number K843265. 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 ID ZINE LD ISOENZYME CONTROL ABNORM?

ID ZINE LD ISOENZYME CONTROL ABNORM is a medical device that received FDA 510(k) clearance on 1984-09-13. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K843265.

When did ID ZINE LD ISOENZYME CONTROL ABNORM receive FDA 510(k) clearance?

ID ZINE LD ISOENZYME CONTROL ABNORM received FDA 510(k) clearance on 1984-09-13, under 510(k) number K843265.

Who is the listed applicant for ID ZINE LD ISOENZYME CONTROL ABNORM?

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 ID ZINE LD ISOENZYME CONTROL ABNORM?

The FDA product code for ID ZINE LD ISOENZYME CONTROL ABNORM 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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