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FDA 510(k)

GORDON IVS INTRAVENOUS STABILIZER

K-Number: K790946 · 1979-06-05

ApplicantWhitman Medical Corp.
Decision Date1979-06-05
Product CodeGBJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GORDON IVS INTRAVENOUS STABILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Whitman Medical Corp.. It received FDA 510(k) clearance on 1979-06-05 under 510(k) number K790946. The device is classified under product code GBJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GORDON IVS INTRAVENOUS STABILIZER?

GORDON IVS INTRAVENOUS STABILIZER is a medical device that received FDA 510(k) clearance on 1979-06-05. The listed applicant is Whitman Medical Corp.. The 510(k) number is K790946.

When did GORDON IVS INTRAVENOUS STABILIZER receive FDA 510(k) clearance?

GORDON IVS INTRAVENOUS STABILIZER received FDA 510(k) clearance on 1979-06-05, under 510(k) number K790946.

Who is the listed applicant for GORDON IVS INTRAVENOUS STABILIZER?

The FDA 510(k) record lists Whitman Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GORDON IVS INTRAVENOUS STABILIZER?

The FDA product code for GORDON IVS INTRAVENOUS STABILIZER is GBJ.

Related Clinical Trials

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Related Devices (Code: GBJ)

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.

K934970DUETTrulife , Ltd.K810282OPERATING TABLE ACCESSORY CLAMPMinnesota Scientific, Inc.K790186PROTECTIVSTABILIZERJelco Laboratories

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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