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FDA 510(k)

PEDIATRIC BLOOD CULTURE BOTTLES

K-Number: K770957 · 1977-06-14

Decision Date1977-06-14
Product CodeJTW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC BLOOD CULTURE BOTTLES 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 1977-06-14 under 510(k) number K770957. 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 PEDIATRIC BLOOD CULTURE BOTTLES?

PEDIATRIC BLOOD CULTURE BOTTLES is a medical device that received FDA 510(k) clearance on 1977-06-14. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K770957.

When did PEDIATRIC BLOOD CULTURE BOTTLES receive FDA 510(k) clearance?

PEDIATRIC BLOOD CULTURE BOTTLES received FDA 510(k) clearance on 1977-06-14, under 510(k) number K770957.

Who is the listed applicant for PEDIATRIC BLOOD CULTURE BOTTLES?

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 PEDIATRIC BLOOD CULTURE BOTTLES?

The FDA product code for PEDIATRIC BLOOD CULTURE BOTTLES is JTW.

Related Clinical Trials

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.

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

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.

View all 67 devices →

Related Devices (Code: JTW)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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