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

SCISSOR - 1.5MM PROBE POINT, ANGLED

K Number: K760792 · Decision Nov 11, 1976
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
41
Review Days
35

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Basic Information

Device Name
SCISSOR - 1.5MM PROBE POINT, ANGLED
K Number
K760792
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Date Received
October 7, 1976
Decision Date
November 11, 1976
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

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Other Clearances by V. Mueller O.V. Baxter Healthcare Corp.

K Number Device Name
K803292 FIELD SUCTION DISSECTOR
K792383 KELMAN DIPSTICK
K771197 NORTON ENDOTRACHEAL
K771302 PFISTER-SCHWARTZ STONE RETRIEVER
K770959 BOUGIE, FILIFORM, JACKSON
K770280 CORD, ELECTROSURGICAL-STERILE & DISPOS.
K760851 CONVERSE ALTAR RETRACTOR
K761242 TEFLON COATED RESECTOSCOPE SHEATH
K760273 LITHOTRITE
K760172 OBTURATOR, VISUAL
Search all 41 clearances from V. Mueller O.V. Baxter Healthcare Corp. →