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

AM. PH. STERILE PLASTIC CONNECTING TUBES

K Number: K820412 · Decision Mar 31, 1982
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
23
Applicant Total
64
Review Days
47

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Basic Information

Device Name
AM. PH. STERILE PLASTIC CONNECTING TUBES
K Number
K820412
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
American Pharmaseal Div. Ahsc
Date Received
February 12, 1982
Decision Date
March 31, 1982
Product Code
BYY
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
BYY Tube, Aspirating, Flexible, Connecting

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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 →