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

MILLS OPERATIVE PERIPHERAL ANGIOPLASTY CATHETER

K Number: K850760 · Decision Apr 10, 1985
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
402
Applicant Total
109
Review Days
44

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Basic Information

Device Name
MILLS OPERATIVE PERIPHERAL ANGIOPLASTY CATHETER
K Number
K850760
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Scimed Life Systems, Inc.
Date Received
February 25, 1985
Decision Date
April 10, 1985
Product Code
LIT
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
LIT Catheter, Angioplasty, Peripheral, Transluminal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LIT), ordered by most recent decision date.

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Other Clearances by Scimed Life Systems, Inc.

K Number Device Name
K974241 SCIMED INFORMER PRESSURE WIRE SYSTEM
K981788 SCIMED 6 FRENCH WISEGUIDE GUIDE CATHETER
K980360 SCIMED QUEST FLOPPY AND MODERATE SUPPORT GUIDE WIRES
K974559 SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS
K974684 SCIMED 7 FRENCH WISEGUIDE GUIDE CATHETER
K973945 LUGE GUIDE WIRE
K970823 SCIMED 8 FRENCH WISEGUIDE GUIDE CATHETER
K964551 CHOICE SUPER SUPPORT PTCA GUIDE WIRE, CHOICE PLUS SUPER SUPPORT PTCA GUIDE WIRE, CHOICE EXCHANGE SUPER SUPPORT PTCA GUID
K970244 SCIMED CHOICE FAMILY OF PTCA GUIDE WIRES
K965023 CHOICE PT PLUS PTCA GUIDE WIRE AND CHOICE PT VISION PTCA GUIDE WIRE
Search all 109 clearances from Scimed Life Systems, Inc. →