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TORAY INOUE BALLOON CATHETER

FDA premarket approval P910054/S005 · decided 2011-05-17

Approval details

PMA number
P910054
Supplement
S005
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
TORAY INOUE BALLOON CATHETER
Generic name
CATHETER, PERCUTANEOUS (VALVULOPLASTY)
Applicant
Toray Industries (America), Inc.
Date received
2011-04-19
Decision date
2011-05-17
Days to decision
28 days
Decision code
OK30
Product code
MAD
Advisory committee
Cardiovascular
Expedited review
No
Location
New York, NY
Statement
ADDITION OF A STERILIZER AT YOUR SETA PLANT FACILITY.

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510(k) clearances by this applicant

RecordFirmDate
TORAYGUIDE GUIDEWIRE (K042370)Toray Industries (America), Inc.2004-12-17
TORAYSULFONE DIALYZER, BS-L SERIES (K030050)Toray Industries (America), Inc.2003-09-29
TORAYSULFONE DIALYZER (K002512)Toray Industries (America), Inc.2001-10-15
HEMOFEEL-CH, MODELS CH-0.35L, CH-0.6L, CH-1.0L (K994198)Toray Industries (America), Inc.2000-08-25
FILTRYZER (K942681)Toray Industries (America), Inc.1995-06-22
FILTRYZER(TM) (K935471)Toray Industries (America), Inc.1995-05-19
FILTRYZER (K940910)Toray Industries (America), Inc.1995-05-04
TORAY FILTRYZER DIALYZERS (K884339)Toray Industries (America), Inc.1989-03-17