The following data is part of a premarket notification filed by American Medical Plastics Co. with the FDA for Amer. Medical Plastics Co 20100.
| Device ID | K842492 |
| 510k Number | K842492 |
| Device Name: | AMER. MEDICAL PLASTICS CO 20100 |
| Classification | Circuit, Breathing (w Connector, Adaptor, Y Piece) |
| Applicant | AMERICAN MEDICAL PLASTICS CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CAI |
| CFR Regulation Number | 868.5240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-06-26 |
| Decision Date | 1984-07-06 |