Contura Dispos. Surg. Face Mask

FDA 510(k) K813078 · American Convertors Div., American Pharmaseal

Substantially Equivalent

510(k) numberK813078

Submission

Device name
Contura Dispos. Surg. Face Mask
Applicant
American Convertors Div., American Pharmaseal
Mchenry, IL, US
Received
November 2, 1981
Decision date
December 18, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FXX – Mask, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

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Questions and answers

When was Contura Dispos. Surg. Face Mask cleared by the FDA?

Contura Dispos. Surg. Face Mask (K813078) received a 510(k) decision of Substantially Equivalent on December 18, 1981, 46 days after the submission was received.

What is the product code of K813078?

The FDA product code is FXX – Mask, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.