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FDA 510(k)

PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM

K-Number: K864755 · 1987-01-05

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1987-01-05
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM 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 1987-01-05 under 510(k) number K864755. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM?

PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM is a medical device that received FDA 510(k) clearance on 1987-01-05. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K864755.

When did PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM receive FDA 510(k) clearance?

PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM received FDA 510(k) clearance on 1987-01-05, under 510(k) number K864755.

Who is the listed applicant for PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM?

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 PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM?

The FDA product code for PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORM is JSJ.

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Related Devices (Code: JSJ)

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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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