Devilbiss Model 6305D Heavy Duty Ac Aspirator

FDA 510(k) K981602 · Sunrise Medical Hhg, Inc.

Substantially Equivalent

510(k) numberK981602

Submission

Device name
Devilbiss Model 6305D Heavy Duty Ac Aspirator
Applicant
Sunrise Medical Hhg, Inc.
Somerset, PA, US
Received
May 5, 1998
Decision date
July 17, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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Questions and answers

When was Devilbiss Model 6305D Heavy Duty Ac Aspirator cleared by the FDA?

Devilbiss Model 6305D Heavy Duty Ac Aspirator (K981602) received a 510(k) decision of Substantially Equivalent on July 17, 1998, 73 days after the submission was received.

What is the product code of K981602?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.