FDA 510(k)

CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE

K-Number: K831219 · 1983-05-13

ApplicantGibco Laboratories Life Technologies, Inc.

Decision Date1983-05-13

Product CodeJSK

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE 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 1983-05-13 under 510(k) number K831219. 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 CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE?

CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE is a medical device that received FDA 510(k) clearance on 1983-05-13. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K831219.

When did CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE receive FDA 510(k) clearance?

CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE received FDA 510(k) clearance on 1983-05-13, under 510(k) number K831219.

Who is the listed applicant for CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE?

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 CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE?

The FDA product code for CLOSTRIDIUM DIFFICILE SELECTIVE SUPPLE is JSK.

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

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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.