The following data is part of a premarket notification filed by Ballard Medical Products with the FDA for Ballard Medical Products Epidural And Spinal Needles.
Device ID | K000495 |
510k Number | K000495 |
Device Name: | BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES |
Classification | Needle, Conduction, Anesthetic (w/wo Introducer) |
Applicant | BALLARD MEDICAL PRODUCTS 12050 LONE PEAK PKWY. Draper, UT 84020 |
Contact | E. Martin Chamberlain |
Correspondent | E. Martin Chamberlain BALLARD MEDICAL PRODUCTS 12050 LONE PEAK PKWY. Draper, UT 84020 |
Product Code | BSP |
CFR Regulation Number | 868.5150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-02-15 |
Decision Date | 2000-03-28 |