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FDA 510(k)

BOTTLE, BLOOD CULTURE, BI-PHASIC

K-Number: K770683 · 1977-04-26

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1977-04-26
Product CodeJTW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BOTTLE, BLOOD CULTURE, BI-PHASIC 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 1977-04-26 under 510(k) number K770683. The device is classified under product code JTW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOTTLE, BLOOD CULTURE, BI-PHASIC?

BOTTLE, BLOOD CULTURE, BI-PHASIC is a medical device that received FDA 510(k) clearance on 1977-04-26. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K770683.

When did BOTTLE, BLOOD CULTURE, BI-PHASIC receive FDA 510(k) clearance?

BOTTLE, BLOOD CULTURE, BI-PHASIC received FDA 510(k) clearance on 1977-04-26, under 510(k) number K770683.

Who is the listed applicant for BOTTLE, BLOOD CULTURE, BI-PHASIC?

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 BOTTLE, BLOOD CULTURE, BI-PHASIC?

The FDA product code for BOTTLE, BLOOD CULTURE, BI-PHASIC is JTW.

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Related Devices (Code: JTW)

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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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