The following data is part of a premarket notification filed by Buckman Co., Inc. with the FDA for Acromed Screw Driver.
Device ID | K873066 |
510k Number | K873066 |
Device Name: | ACROMED SCREW DRIVER |
Classification | Screwdriver |
Applicant | BUCKMAN CO., INC. 921 CALLE VERDE Martinez, CA 94553 |
Contact | David W Schlerf |
Correspondent | David W Schlerf BUCKMAN CO., INC. 921 CALLE VERDE Martinez, CA 94553 |
Product Code | HXX |
CFR Regulation Number | 888.4540 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-08-05 |
Decision Date | 1987-09-02 |