The following data is part of a premarket notification filed by Medical Safety Products, Inc. with the FDA for Acci-guard Multi-sample Blood Collection Needle.
Device ID | K881654 |
510k Number | K881654 |
Device Name: | ACCI-GUARD MULTI-SAMPLE BLOOD COLLECTION NEEDLE |
Classification | Needle, Hypodermic, Single Lumen |
Applicant | MEDICAL SAFETY PRODUCTS, INC. 2696 S. COLORADO BLVD., SUITE 585 Denver, CO 80222 |
Contact | William Sagstetter |
Correspondent | William Sagstetter MEDICAL SAFETY PRODUCTS, INC. 2696 S. COLORADO BLVD., SUITE 585 Denver, CO 80222 |
Product Code | FMI |
CFR Regulation Number | 880.5570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-04-15 |
Decision Date | 1988-07-08 |