National Biological Corp.
National Biological Corp. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2007, with 3 FDA device recalls on record.
Top product codes for National Biological Corp.
FDA recalls by National Biological Corp.
- Z-1683-2017 — Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment.
- Z-1778-2013 — Dermalight 80 Model Number UVB-080, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo.
- Z-1779-2013 — Dermalight 80 Model Number UVB-083, one unit per box. The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by National Biological Corp.
- K070934 — PANOSOL II TRU-BLU, MODEL UBL-417
- K041212 — HOUVA 3 PHOTOTHERAPY SYSTEM
- K982082 — HANDISOL WOUND HEALING
- K934808 — UVISOL AND UVISOL II
- K924969 — PHOTOTHERAPY TIMER
- K924077 — HANDISOL
- K904426 — PANOSOL II UVA-218
- K904427 — PANOSOL II UVB-206
- K904428 — PANOSOL II UAB-228
- K885026 — HOUVA II UVB
- K885029 — HOUVA II UVA/UVB
- K885025 — HOUVA II UVA
- K882722 — HOUVA-BED
- K872649 — HAND/FOOT UVA/UVB 624-224
- K872650 — PANOSOL 2000 624-604
- K872651 — PANOSOL 2000 624-414
- K872706 — PANOSOL 2000 624-616
- K872707 — PANOSOL 2000 624-404
- K872604 — HAND/FOOT 624-208
- K872605 — HAND/FOOT UVA 624-218
- K864546 — MAXI-TAN DEVICE
- K827890 — FOLDALITE UNIT
- K810668 — HO-B-LITE VI UNIT
- K761186 — HOUVA-LITE ARM UNIT #601
- K761187 — HOUVA-LITE LEG UNIT #701
- K761188 — HOUVA-LITE PALM UNIT #501
- K761189 — HOUVA-LITE SOLE UNIT #502
Data sourced from openFDA. This site is unofficial and independent of the FDA.