American Medical Devices, Inc. · Class I · Cleared Feb 19, 1998
| K-number | K974561 |
| Device name | MOISTAIR FLUID AIR TUBING SET |
| Applicant | American Medical Devices, Inc. |
| Product code | KYG |
| Device class | Class I |
| Decision date | Feb 19, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 886.4360 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov