IP-16

FDA 510(k) K980301 · Servizi Medico Estetici Italinai Srl.

Substantially Equivalent

510(k) numberK980301

Submission

Device name
IP-16
Applicant
Servizi Medico Estetici Italinai Srl.
Morristown, TN, US
Received
January 27, 1998
Decision date
March 24, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 IP-16 cleared by the FDA?

IP-16 (K980301) received a 510(k) decision of Substantially Equivalent on March 24, 1998, 56 days after the submission was received.

What is the product code of K980301?

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