The following data is part of a premarket notification filed by Dale Medical Products, Inc. with the FDA for Dale I.v. Connect. Lock & Stabilizer (stabilok)220.
Device ID | K873311 |
510k Number | K873311 |
Device Name: | DALE I.V. CONNECT. LOCK & STABILIZER (STABILOK)220 |
Classification | Device, Intravascular Catheter Securement |
Applicant | DALE MEDICAL PRODUCTS, INC. 7 CROSS ST. P.O. BOX 1556 Plainville, MA 02762 |
Contact | Daniel W Mcelaney |
Correspondent | Daniel W Mcelaney DALE MEDICAL PRODUCTS, INC. 7 CROSS ST. P.O. BOX 1556 Plainville, MA 02762 |
Product Code | KMK |
CFR Regulation Number | 880.5210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-17 |
Decision Date | 1987-11-05 |