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FDA 510(k)

DRI-FORM PSEUDOMONAS AGAR F

K-Number: K852064 · 1985-06-04

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1985-06-04
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DRI-FORM PSEUDOMONAS AGAR F 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 1985-06-04 under 510(k) number K852064. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRI-FORM PSEUDOMONAS AGAR F?

DRI-FORM PSEUDOMONAS AGAR F is a medical device that received FDA 510(k) clearance on 1985-06-04. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K852064.

When did DRI-FORM PSEUDOMONAS AGAR F receive FDA 510(k) clearance?

DRI-FORM PSEUDOMONAS AGAR F received FDA 510(k) clearance on 1985-06-04, under 510(k) number K852064.

Who is the listed applicant for DRI-FORM PSEUDOMONAS AGAR F?

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 DRI-FORM PSEUDOMONAS AGAR F?

The FDA product code for DRI-FORM PSEUDOMONAS AGAR F is JSH.

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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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