The following data is part of a premarket notification filed by Angiosystems, Inc. with the FDA for Medical Procedure Kits/arterial Blood Sampling.
| Device ID | K905464 |
| 510k Number | K905464 |
| Device Name: | MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING |
| Classification | Arterial Blood Sampling Kit |
| Applicant | ANGIOSYSTEMS, INC. C/O MEDICAL DEVICE INSPECITON 55 NORTHERN BLVD., SUITE 301 Great Neck, NY 11021 |
| Contact | Alan P Schwartz |
| Correspondent | Alan P Schwartz ANGIOSYSTEMS, INC. C/O MEDICAL DEVICE INSPECITON 55 NORTHERN BLVD., SUITE 301 Great Neck, NY 11021 |
| Product Code | CBT |
| CFR Regulation Number | 868.1100 [🔎] |
| Decision | Substantially Equivalent - Kit With Drugs (SEKD) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-12-05 |
| Decision Date | 1991-05-31 |