The following data is part of a premarket notification filed by Aesculap Instruments Corp. with the FDA for Caspar Scalp Clip, Applier.
| Device ID | K890443 |
| 510k Number | K890443 |
| Device Name: | CASPAR SCALP CLIP, APPLIER |
| Classification | Clip, Scalp |
| Applicant | AESCULAP INSTRUMENTS CORP. 875 STANTON RD. Burlingame, CA 94010 |
| Contact | Robin Bush |
| Correspondent | Robin Bush AESCULAP INSTRUMENTS CORP. 875 STANTON RD. Burlingame, CA 94010 |
| Product Code | HBO |
| CFR Regulation Number | 882.4150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-27 |
| Decision Date | 1989-06-15 |