Laerdal Alternative Power, 5-6 A,5-6 B,2000

FDA 510(k) K930549 · Rustronics, Inc.

Substantially Equivalent

510(k) numberK930549

Submission

Device name
Laerdal Alternative Power, 5-6 A,5-6 B,2000
Applicant
Rustronics, Inc.
Pt. St. Lucie, FL, US
Received
February 3, 1993
Decision date
June 18, 1993
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 Laerdal Alternative Power, 5-6 A,5-6 B,2000 cleared by the FDA?

Laerdal Alternative Power, 5-6 A,5-6 B,2000 (K930549) received a 510(k) decision of Substantially Equivalent on June 18, 1993, 135 days after the submission was received.

What is the product code of K930549?

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