FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AMERICAN PHARMASEAL TRIPLE LUMEN CATHETER

K Number: K852491 · Decision Sep 25, 1985
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
64
Review Days
105

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Basic Information

Device Name
AMERICAN PHARMASEAL TRIPLE LUMEN CATHETER
K Number
K852491
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
American Pharmaseal Div. Ahsc
Date Received
June 12, 1985
Decision Date
September 25, 1985
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DQY Catheter, Percutaneous

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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 →