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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name regulator, pressure, gas cylinder
510(k) Number K810132
Device Name MODEL 2 FLOWMETER
Applicant
HARRIS CALORIFIC
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
HARRIS CALORIFIC
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.2700
Classification Product Code
CAN  
Date Received01/19/1981
Decision Date 01/28/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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