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

CATHETER, DOVER SUCTION W/ GLOVE

K Number: K760427 · Decision Sep 9, 1976
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
14
Review Days
27

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Basic Information

Device Name
CATHETER, DOVER SUCTION W/ GLOVE
K Number
K760427
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Will Ross Co.
Date Received
August 13, 1976
Decision Date
September 9, 1976
Product Code
BSY
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
BSY Catheters, Suction, Tracheobronchial

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Other Clearances by Will Ross Co.

K Number Device Name
K780850 SEARLE NEONATAL OXYGEN PROBE
K771561 DOVER URINE METER
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
Search all 14 clearances from Will Ross Co. →