The following data is part of a premarket notification filed by Critical Care Micro Computing with the FDA for Guidelines For Pediatric Anesthesia.
| Device ID | K842610 |
| 510k Number | K842610 |
| Device Name: | GUIDELINES FOR PEDIATRIC ANESTHESIA |
| Classification | Apparatus, Autotransfusion |
| Applicant | CRITICAL CARE MICRO COMPUTING 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAC |
| CFR Regulation Number | 868.5830 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-07-05 |
| Decision Date | 1984-10-04 |