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

DIMENSIONALL ROTATOR

K Number: K790753 · Decision Jun 28, 1979
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
7
Applicant Total
56
Review Days
72

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Basic Information

Device Name
DIMENSIONALL ROTATOR
K Number
K790753
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
American Hospital Supply Corp.
Date Received
April 17, 1979
Decision Date
June 28, 1979
Product Code
JRQ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
JRQ Shaker/Stirrer

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Other Clearances by American Hospital Supply Corp.

K Number Device Name
K854739 AMERICAN STERILE SURGICAL ABSORBENT TOWEL
K854759 AMERICAN STERILE MAYO STAND TRAY
K832826 AAP DOSIMETRY RELEASE OR BASIN SETS
K830546 DOSIMETRIC RELEASE
K822990 CONVERTORS PRIMARY WOUND DRESSING II
K830343 CONTAINER W/PRIMING SOLUTION
K830301 STRATUS FLUOROMETRIC ENZYME IMMUN0-
K822755 LATEX PENROSE TUBING
K823418 HEYER-SCHUTE UNIVERSAL URETERAL STENT
K822966 CONVERTORS DISPOSABLE DRESSING SPONGE
Search all 56 clearances from American Hospital Supply Corp. →