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FDA 510(k)

MIDDLEBROOK ADC ENRICHMENT

K-Number: K832902 · 1983-09-26

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1983-09-26
Product CodeJSK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MIDDLEBROOK ADC ENRICHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832902. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDDLEBROOK ADC ENRICHMENT?

MIDDLEBROOK ADC ENRICHMENT is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K832902.

When did MIDDLEBROOK ADC ENRICHMENT receive FDA 510(k) clearance?

MIDDLEBROOK ADC ENRICHMENT received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832902.

Who is the listed applicant for MIDDLEBROOK ADC ENRICHMENT?

The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIDDLEBROOK ADC ENRICHMENT?

The FDA product code for MIDDLEBROOK ADC ENRICHMENT is JSK.

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Other records listing Gibco Laboratories Life Technologies, Inc. as applicant

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Related Devices (Code: JSK)

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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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