The following data is part of a premarket notification filed by Target Therapeutics with the FDA for Zephyr Infusion Catheter.
Device ID | K921247 |
510k Number | K921247 |
Device Name: | ZEPHYR INFUSION CATHETER |
Classification | Catheter, Continuous Flush |
Applicant | TARGET THERAPEUTICS 47201 LAKEVIEW BLVD. P.O. BOX 5120 Freemont, CA 94538 |
Contact | Craig J Coombs |
Correspondent | Craig J Coombs TARGET THERAPEUTICS 47201 LAKEVIEW BLVD. P.O. BOX 5120 Freemont, CA 94538 |
Product Code | KRA |
CFR Regulation Number | 870.1210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-03-16 |
Decision Date | 1993-06-29 |