Anaeslock Three Vaporizer Interlock HVA003

FDA 510(k) K843993 · Southmedic, Inc.

Substantially Equivalent

510(k) numberK843993

Submission

Device name
Anaeslock Three Vaporizer Interlock HVA003
Applicant
Southmedic, Inc.
Ancaster, Ontario, CA
Received
October 11, 1984
Decision date
November 15, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAD – Vaporizer, Anesthesia, Non-Heated
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5880
Specialty
Anesthesiology

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Questions and answers

When was Anaeslock Three Vaporizer Interlock HVA003 cleared by the FDA?

Anaeslock Three Vaporizer Interlock HVA003 (K843993) received a 510(k) decision of Substantially Equivalent on November 15, 1984, 35 days after the submission was received.

What is the product code of K843993?

The FDA product code is CAD – Vaporizer, Anesthesia, Non-Heated, a Class II (moderate risk) device regulated under 21 CFR 868.5880.