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

DOVER URINE METER

K Number: K771561 · Decision Sep 7, 1977
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
8
Applicant Total
14
Review Days
23

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Basic Information

Device Name
DOVER URINE METER
K Number
K771561
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1800
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Will Ross Co.
Date Received
August 15, 1977
Decision Date
September 7, 1977
Product Code
EXR
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
EXR Urinometer, Mechanical

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Other Clearances by Will Ross Co.

K Number Device Name
K780850 SEARLE NEONATAL OXYGEN PROBE
K771132 KENWOOD BIOLOGICAL STEOILIZ. INDICATOR
K770611 PARALLEL BARS
K770612 SPLINT, BOHLER
K770607 TRACTION HARNESS
K770608 WALKING AID
K770610 TABLE, TREATMENT & TRACTION, HI-LO
K770609 TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT
K770509 TABLE, MASSAGE AND TREATMENT
K770399 VALVE FOR CLOSED SYS. URINARY DRAINAGE
Search all 14 clearances from Will Ross Co. →