Carotid Artery Clamp W/Pilling LMM

FDA 510(k) K760646 · Pilling Co.

Substantially Equivalent

510(k) numberK760646

Submission

Device name
Carotid Artery Clamp W/Pilling LMM
Applicant
Pilling Co.
Mchenry, IL, US
Received
September 15, 1976
Decision date
September 21, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DWS – Instruments, Surgical, Cardiovascular
Device class
Class I (low risk)
Regulation
21 CFR 870.4500
Specialty
Cardiovascular

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Questions and answers

When was Carotid Artery Clamp W/Pilling LMM cleared by the FDA?

Carotid Artery Clamp W/Pilling LMM (K760646) received a 510(k) decision of Substantially Equivalent on September 21, 1976, 6 days after the submission was received.

What is the product code of K760646?

The FDA product code is DWS – Instruments, Surgical, Cardiovascular, a Class I (low risk) device regulated under 21 CFR 870.4500.