Trantec Disposable Pressure TRANS.53-600/F/F30

FDA 510(k) K872596 · American Edwards Laboratories

Substantially Equivalent

510(k) numberK872596

Submission

Device name
Trantec Disposable Pressure TRANS.53-600/F/F30
Applicant
American Edwards Laboratories
Santa Ana, CA, US
Received
July 2, 1987
Decision date
September 30, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DRS – Transducer, Blood-Pressure, Extravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2850
Specialty
Cardiovascular

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Questions and answers

When was Trantec Disposable Pressure TRANS.53-600/F/F30 cleared by the FDA?

Trantec Disposable Pressure TRANS.53-600/F/F30 (K872596) received a 510(k) decision of Substantially Equivalent on September 30, 1987, 90 days after the submission was received.

What is the product code of K872596?

The FDA product code is DRS – Transducer, Blood-Pressure, Extravascular, a Class II (moderate risk) device regulated under 21 CFR 870.2850.