Company · US
Prestige Ameritech
FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2024. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 5, 2024 | K231741 | ProGear® Surgical Mask with Oxafence®, Model AV82030 Prestige Ameritech | OUK |
| Aug 15, 2017 | K171162 | Surgical Earloop Face Mask with Bottom Gap Shield and Surgical Tie-On Face Mask with Bottom Gap Shield Prestige Ameritech | FXX |
| Oct 7, 2016 | K160100 | Prestige Ameritech Pediatric/Childs Face mask Prestige Ameritech | OXZ |
| Jun 3, 2016 | K152561 | Communicator Surgical Facemask with Clear Window Prestige Ameritech , Ltd. | FXX |
| Oct 6, 2010 | K102092 | PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES Prestige Ameritech | MSH |
| Aug 14, 2006 | K061716 | PRESTIGE AMERITECH FACE MASK Prestige Ameritech | FXX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||