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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, Tubing And Support, Ventilator (W Harness)
510(k) Number K820131
Device Name 3M VOLUME VENTIATOR CIRCUIT
Applicant
3M Company
2724 S. Peck Rd.
Monrovia,  CA  91016
Correspondent
3M Company
2724 S. Peck Rd.
Monrovia,  CA  91016
Regulation Number868.5975
Classification Product Code
BZO  
Date Received01/18/1982
Decision Date 01/28/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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