Prima Anaesthesia Machine

FDA 510(k) K061102 · Penlon , Ltd.

Substantially Equivalent

510(k) numberK061102

Submission

Device name
Prima Anaesthesia Machine
Applicant
Penlon , Ltd.
Barton Lane, Abingdon, GB
Received
April 19, 2006
Decision date
July 28, 2006
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BSZ – Gas-Machine, Anesthesia
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5160
Specialty
Anesthesiology
Life-sustaining
Yes

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Questions and answers

When was Prima Anaesthesia Machine cleared by the FDA?

Prima Anaesthesia Machine (K061102) received a 510(k) decision of Substantially Equivalent on July 28, 2006, 100 days after the submission was received.

What is the product code of K061102?

The FDA product code is BSZ – Gas-Machine, Anesthesia, a Class II (moderate risk) device regulated under 21 CFR 868.5160.