The following data is part of a premarket notification filed by Wildcat Medical, Inc. with the FDA for Tripleplay Pro.
| Device ID | K141360 |
| 510k Number | K141360 |
| Device Name: | TRIPLEPLAY PRO |
| Classification | Sleeve, Limb, Compressible |
| Applicant | WILDCAT MEDICAL, INC. 1638 S. MAIN STREET Tulsa, OK 74119 |
| Contact | Mike Bartlett |
| Correspondent | Mike Bartlett WILDCAT MEDICAL, INC. 1638 S. MAIN STREET Tulsa, OK 74119 |
| Product Code | JOW |
| CFR Regulation Number | 870.5800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-05-23 |
| Decision Date | 2014-06-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04042809585872 | K141360 | 000 |
| 04042809585865 | K141360 | 000 |