Atlas FDA

Inoue-Balloon Catheter

FDA premarket approval P910054/S009 · decided 2024-05-24

Approval details

PMA number
P910054
Supplement
S009
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Inoue-Balloon Catheter
Generic name
CATHETER, PERCUTANEOUS (VALVULOPLASTY)
Applicant
Toray Industries (America), Inc.
Date received
2023-10-31
Decision date
2024-05-24
Days to decision
206 days
Decision code
APPR
Product code
MAD
Advisory committee
Cardiovascular
Expedited review
No
Location
New York, NY
Statement
approval for the use of packaging pouches with a change in the specification of a film component, the use of a new plasma welding machine for an accessory device, and the use of a new plating company for the plating of the hubs of device components.

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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