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FDA 510(k)

PSEUDOMONAS AGAR P (MEDIUM A)

K-Number: K860750 · 1986-03-10

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1986-03-10
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PSEUDOMONAS AGAR P (MEDIUM A) 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 1986-03-10 under 510(k) number K860750. 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 PSEUDOMONAS AGAR P (MEDIUM A)?

PSEUDOMONAS AGAR P (MEDIUM A) is a medical device that received FDA 510(k) clearance on 1986-03-10. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K860750.

When did PSEUDOMONAS AGAR P (MEDIUM A) receive FDA 510(k) clearance?

PSEUDOMONAS AGAR P (MEDIUM A) received FDA 510(k) clearance on 1986-03-10, under 510(k) number K860750.

Who is the listed applicant for PSEUDOMONAS AGAR P (MEDIUM A)?

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 AGAR P (MEDIUM A)?

The FDA product code for PSEUDOMONAS AGAR P (MEDIUM A) is JSH.

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

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Related Devices (Code: JSH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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