Specimen Collector, Anaerobic

FDA 510(k) K760063 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK760063

Submission

Device name
Specimen Collector, Anaerobic
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Washington, DC, US
Received
June 16, 1976
Decision date
August 3, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JTX – Transport Systems, Anaerobic
Device class
Class I (low risk)
Regulation
21 CFR 866.2900
Specialty
Microbiology

Other 510(k)s with product code JTX

510(k)DeviceApplicantDecision
K901645Anaerobic Accu-Culshure(Tm)JTX · Traditional Medical Laboratory Automation Systems, Inc.07/16/1990SE
K897151Acuson V328 and C5432 TransducersJTX · Traditional Acuson Corp.07/03/1990SE
K882637Accu-Culshure TMJTX · Traditional Accu-Med Corp.07/06/1988SE
K791724Bio-Bag Environmental Chamber (a & B)JTX · Traditional Marion Laboratories, Inc.10/17/1979SE
K781376Standardize TGCL & TGCHJTX · Traditional American Monitor Corp.09/14/1978SE
K780159AnaswabJTX · Traditional Scott Laboratories, Inc.02/13/1978SE
K761241Pre-Duced Surgi-Swab & Transporter TubeJTX · Traditional Gibco Laboratories Life Technologies, Inc.12/30/1976SE

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Questions and answers

When was Specimen Collector, Anaerobic cleared by the FDA?

Specimen Collector, Anaerobic (K760063) received a 510(k) decision of Substantially Equivalent on August 3, 1976, 48 days after the submission was received.

What is the product code of K760063?

The FDA product code is JTX – Transport Systems, Anaerobic, a Class I (low risk) device regulated under 21 CFR 866.2900.