The following data is part of a premarket notification filed by Scimed Life Systems, Inc. with the FDA for Scimed(r) Chice(tm) Exchange Ptca Guide Wire.
Device ID | K950113 |
510k Number | K950113 |
Device Name: | SCIMED(R) CHICE(TM) EXCHANGE PTCA GUIDE WIRE |
Classification | Wire, Guide, Catheter |
Applicant | SCIMED LIFE SYSTEMS, INC. 2010 EAST CENTER CIRCLE Plymouth, MN 55441 -2644 |
Contact | Deborah L Jensen |
Correspondent | Deborah L Jensen SCIMED LIFE SYSTEMS, INC. 2010 EAST CENTER CIRCLE Plymouth, MN 55441 -2644 |
Product Code | DQX |
CFR Regulation Number | 870.1330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-01-11 |
Decision Date | 1995-03-31 |