The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Monoject Whitacre Point Spinal Needle (27g X 3 1/2).
Device ID | K951312 |
510k Number | K951312 |
Device Name: | MONOJECT WHITACRE POINT SPINAL NEEDLE (27G X 3 1/2) |
Classification | Needle, Conduction, Anesthetic (w/wo Introducer) |
Applicant | SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
Contact | K. M Kroehnke |
Correspondent | K. M Kroehnke SHERWOOD MEDICAL CO. 1915 OLIVE ST. St. Louis, MO 63103 -1625 |
Product Code | BSP |
CFR Regulation Number | 868.5150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-03-23 |
Decision Date | 1995-05-03 |