The following data is part of a premarket notification filed by Plasco, Inc. with the FDA for Cpr Micromask Plus Catalog No 73-402.
| Device ID | K950769 |
| 510k Number | K950769 |
| Device Name: | CPR MICROMASK PLUS CATALOG NO 73-402 |
| Classification | Valve, Non-rebreathing |
| Applicant | PLASCO, INC. 4080 MORRISON DR. Gurnee, IL 60031 |
| Contact | Gary S Botsford |
| Correspondent | Gary S Botsford PLASCO, INC. 4080 MORRISON DR. Gurnee, IL 60031 |
| Product Code | CBP |
| CFR Regulation Number | 868.5870 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-21 |
| Decision Date | 1995-03-10 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00347682807009 | K950769 | 000 |
| 50748426074476 | K950769 | 000 |
| 50748426075107 | K950769 | 000 |
| 50748426075114 | K950769 | 000 |
| 50748426075138 | K950769 | 000 |
| 50748426075152 | K950769 | 000 |
| 50748426075299 | K950769 | 000 |
| 50748426078320 | K950769 | 000 |
| 50748426074407 | K950769 | 000 |
| 50748426120395 | K950769 | 000 |
| 50748426121071 | K950769 | 000 |
| 50748426121088 | K950769 | 000 |
| 50748426121118 | K950769 | 000 |
| 50748426121125 | K950769 | 000 |
| 50748426121132 | K950769 | 000 |
| 30748426121169 | K950769 | 000 |
| 50748426075411 | K950769 | 000 |
| 50748426074469 | K950769 | 000 |