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FDA 510(k)

BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2

K-Number: K790687 · 1979-05-03

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1979-05-03
Product CodeJSC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2 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 1979-05-03 under 510(k) number K790687. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2?

BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2 is a medical device that received FDA 510(k) clearance on 1979-05-03. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K790687.

When did BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2 receive FDA 510(k) clearance?

BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2 received FDA 510(k) clearance on 1979-05-03, under 510(k) number K790687.

Who is the listed applicant for BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2?

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 BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2?

The FDA product code for BRUCELLA BROTH W/SPS, 6% SORBITOL & CO2 is JSC.

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Related Devices (Code: JSC)

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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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