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

SPECIMEN SET

K Number: K802340 · Decision Oct 10, 1980
Classifications
1
FEI Numbers
294
Registration Numbers
294
Same Product Code
22
Applicant Total
64
Review Days
14

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Basic Information

Device Name
SPECIMEN SET
K Number
K802340
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3250
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
American Pharmaseal Div. Ahsc
Date Received
September 26, 1980
Decision Date
October 10, 1980
Product Code
FMH
Advisory Committee
Pathology
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
FMH Container, Specimen, Sterile

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 →