Home › Device types › PDH
Blanket, Neonatal Phototherapy
FDA product code PDH · Class 2 · General Hospital
10
Registered devices
0
Adverse events
1
Recalls
2
510(k) clearances
Devices with this code
ADVANCED PHOTOTHERAPY LAMP — ADVANCED INSTRUMENTATIONS, INC.BIONIX DEVELOPMENT CORPORATION — Bionix, LLCN/A — SALTER LABSBIONIX DEVELOPMENT CORPORATION — M&H Medical Holdings, Inc.N/A — SALTER LABSN/A — SALTER LABSBIONIX DEVELOPMENT CORPORATION — Bionix, LLCSwaddler for Phototherapy — Bionix, LLCSwaddler for Phototherapy — Bionix, LLCBIONIX DEVELOPMENT CORPORATION — M&H Medical Holdings, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-07-11 | Beevers Manufacturing & Supply, Inc. | Beevers Manufacturing & Supply Inc. is recalling Luma Wrap neonatal phototherapy blankets because the product was inadvertently misclassified and marketed witho |
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