The following data is part of a premarket notification filed by David Simmonds Co., Inc. with the FDA for Anesthesia Extension Tubes.
| Device ID | K820527 |
| 510k Number | K820527 |
| Device Name: | ANESTHESIA EXTENSION TUBES |
| Classification | Tubing, Fluid Delivery |
| Applicant | DAVID SIMMONDS CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FPK |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-01 |
| Decision Date | 1982-03-18 |