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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 K860880
Device Name VENTILATOR CIRCUITS (VARIOUS TYPES)
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
DIVISION OF DIEMOLDING CORP.
CANASTOTA,  NY  13032
Applicant Contact RONALD N MCHENRY
Correspondent
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
DIVISION OF DIEMOLDING CORP.
CANASTOTA,  NY  13032
Correspondent Contact RONALD N MCHENRY
Regulation Number868.5975
Classification Product Code
BZO  
Date Received02/25/1986
Decision Date 03/20/1986
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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