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

PHARMASEAL MEDI-VAC INTRA-OPER. AUTOTRANSFUS. KIT

K Number: K861677 · Decision Jun 16, 1986
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
194
Applicant Total
64
Review Days
46

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Basic Information

Device Name
PHARMASEAL MEDI-VAC INTRA-OPER. AUTOTRANSFUS. KIT
K Number
K861677
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5830
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
American Pharmaseal Div. Ahsc
Date Received
May 1, 1986
Decision Date
June 16, 1986
Product Code
CAC
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
CAC Apparatus, Autotransfusion

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 →