510(k) K901362 ยท CAF Nebulizer (Direct Patient Interface)
ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE
| Applicant | Automatic Liquid Packaging, Inc., Woodstock IL, US |
| Decision | Substantially Equivalent, Jun 6, 1990 |
| Received | Mar 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901362
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.