The following data is part of a premarket notification filed by Westmark Enterprises, Inc. with the FDA for Modified C.p.r. Microshield.
| Device ID | K871403 |
| 510k Number | K871403 |
| Device Name: | MODIFIED C.P.R. MICROSHIELD |
| Classification | Airway, Oropharyngeal, Anesthesiology |
| Applicant | WESTMARK ENTERPRISES, INC. 8710 TRUMBULL AVE. Skokie, IL 60076 |
| Contact | Mark D Westfall |
| Correspondent | Mark D Westfall WESTMARK ENTERPRISES, INC. 8710 TRUMBULL AVE. Skokie, IL 60076 |
| Product Code | CAE |
| CFR Regulation Number | 868.5110 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-04-08 |
| Decision Date | 1987-05-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20025715696427 | K871403 | 000 |