Resuscitation Timer, Model L770-CPR

FDA 510(k) K062080 · Allied Healthcare Products, Inc.

Substantially Equivalent

510(k) numberK062080

Submission

Device name
Resuscitation Timer, Model L770-CPR
Applicant
Allied Healthcare Products, Inc.
Saint Louis, MO, US
Received
July 21, 2006
Decision date
October 18, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BTM – Ventilator, Emergency, Manual (Resuscitator)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5915
Specialty
Anesthesiology
Life-sustaining
Yes

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Questions and answers

When was Resuscitation Timer, Model L770-CPR cleared by the FDA?

Resuscitation Timer, Model L770-CPR (K062080) received a 510(k) decision of Substantially Equivalent on October 18, 2006, 89 days after the submission was received.

What is the product code of K062080?

The FDA product code is BTM – Ventilator, Emergency, Manual (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5915.