The following data is part of a premarket notification filed by Continental Medical Laboratories, Inc. with the FDA for Staple Removal Kit.
| Device ID | K963234 |
| 510k Number | K963234 |
| Device Name: | STAPLE REMOVAL KIT |
| Classification | Staple, Removable (skin) |
| Applicant | CONTINENTAL MEDICAL LABORATORIES, INC. 817 W.MOHR AVE. P.O. BOX 306 Waterford, WI 53185 |
| Contact | Joseph Dunn |
| Correspondent | Joseph Dunn CONTINENTAL MEDICAL LABORATORIES, INC. 817 W.MOHR AVE. P.O. BOX 306 Waterford, WI 53185 |
| Product Code | GDT |
| CFR Regulation Number | 878.4760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-08-19 |
| Decision Date | 1996-10-21 |