The following data is part of a premarket notification filed by Armm, Inc. with the FDA for Super-flow Tubing.
| Device ID | K922245 |
| 510k Number | K922245 |
| Device Name: | SUPER-FLOW TUBING |
| Classification | Insufflator, Laparoscopic |
| Applicant | ARMM, INC. 17744 SAMPSON LN. Huntington Beach, CA 92647 |
| Contact | Michal E Hamlin |
| Correspondent | Michal E Hamlin ARMM, INC. 17744 SAMPSON LN. Huntington Beach, CA 92647 |
| Product Code | HIF |
| CFR Regulation Number | 884.1730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-05-13 |
| Decision Date | 1993-09-03 |