The following data is part of a premarket notification filed by American Hospital Supply Corp. with the FDA for Latex Penrose Tubing Cat. #20400,414,416.
| Device ID | K802761 |
| 510k Number | K802761 |
| Device Name: | LATEX PENROSE TUBING CAT. #20400,414,416 |
| Classification | Tubing, Noninvasive |
| Applicant | AMERICAN HOSPITAL SUPPLY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GAZ |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-11-04 |
| Decision Date | 1980-11-19 |