FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

AMERICAN PHARMASEAL HUMIDAIR CONDENSER

K Number: K854012 · Decision Dec 3, 1985
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
64
Review Days
64

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Basic Information

Device Name
AMERICAN PHARMASEAL HUMIDAIR CONDENSER
K Number
K854012
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
American Pharmaseal Div. Ahsc
Date Received
September 30, 1985
Decision Date
December 3, 1985
Product Code
BYD
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BYD Condenser, Heat And Moisture (Artificial Nose)

Similar 510(k) Clearances

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Other Clearances by American Pharmaseal Div. Ahsc

K Number Device Name
K874022 PHARMASEAL WOUND IRRIGATION DEVICE
K874517 PHARMASEAL RUBBER URETHRAL CATHETER
K874045 PHARMASEAL ENDOSCOPY PREP KIT UPPER AND LOWER
K873359 AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE
K872228 PHARMASEAL ALTERNATING PRESSURE PAD SYSTEM
K872917 JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETER
K871429 ANTIMICROBIAL FOLEY CATHETER
K871770 AMERICAN PHARMASEAL WOUND DRESSING
K870387 EUROMEDICAL, ENDOSOFT ENDOTRACHEAL TUBE
K870977 PHARMASEAL T TYPE THERMOCOUPLE 100% CATH./PROBE
Search all 64 clearances from American Pharmaseal Div. Ahsc →