Bronchoscope Suction Unit

FDA 510(k) K841399 · Keymed, Inc.

Substantially Equivalent

510(k) numberK841399

Submission

Device name
Bronchoscope Suction Unit
Applicant
Keymed, Inc.
Mchenry, IL, US
Received
April 3, 1984
Decision date
July 18, 1984
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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Questions and answers

When was Bronchoscope Suction Unit cleared by the FDA?

Bronchoscope Suction Unit (K841399) received a 510(k) decision of Substantially Equivalent on July 18, 1984, 106 days after the submission was received.

What is the product code of K841399?

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