Emergency Aspirator

FDA 510(k) K833785 · Vitalograph , Ltd.

Substantially Equivalent

510(k) numberK833785

Submission

Device name
Emergency Aspirator
Applicant
Vitalograph , Ltd.
Mchenry, IL, US
Received
October 28, 1983
Decision date
December 22, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K925085Escort SpirometerBZG · Traditional 08/12/1993SE
K930085Vitalograph Data Storage SpirometerBTY · Traditional 07/26/1993SE
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Questions and answers

When was Emergency Aspirator cleared by the FDA?

Emergency Aspirator (K833785) received a 510(k) decision of Substantially Equivalent on December 22, 1983, 55 days after the submission was received.

What is the product code of K833785?

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