The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Bardex Lubri-sil All-silicone Lubricious Coated Foley Catheter 6 Fr.
Device ID | K070508 |
510k Number | K070508 |
Device Name: | BARDEX LUBRI-SIL ALL-SILICONE LUBRICIOUS COATED FOLEY CATHETER 6 FR |
Classification | Catheter, Retention Type, Balloon |
Applicant | C.R. BARD, INC. 8195 INDUSTRIAL BLVD. Covington, GA 30014 |
Contact | Michelle Gudith |
Correspondent | Robert Mosenkis CITECH 5200 BUTLER PIKE Plymouth Meeting, PA 19462 -1298 |
Product Code | EZL |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2007-02-22 |
Decision Date | 2007-03-09 |
Summary: | summary |