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FDA 510(k)

MIDDLEBROOK 7H10 AGAR BASE-LOWPH

K-Number: K823859 · 1983-03-08

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1983-03-08
Product CodeMJD
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MIDDLEBROOK 7H10 AGAR BASE-LOWPH 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 1983-03-08 under 510(k) number K823859. The device is classified under product code MJD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDDLEBROOK 7H10 AGAR BASE-LOWPH?

MIDDLEBROOK 7H10 AGAR BASE-LOWPH is a medical device that received FDA 510(k) clearance on 1983-03-08. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K823859.

When did MIDDLEBROOK 7H10 AGAR BASE-LOWPH receive FDA 510(k) clearance?

MIDDLEBROOK 7H10 AGAR BASE-LOWPH received FDA 510(k) clearance on 1983-03-08, under 510(k) number K823859.

Who is the listed applicant for MIDDLEBROOK 7H10 AGAR BASE-LOWPH?

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 7H10 AGAR BASE-LOWPH?

The FDA product code for MIDDLEBROOK 7H10 AGAR BASE-LOWPH is MJD.

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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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