FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HOUVA-LITE ARM UNIT #601

K Number: K761186 · Decision Feb 28, 1977
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
271
Applicant Total
27
Review Days
84

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Basic Information

Device Name
HOUVA-LITE ARM UNIT #601
K Number
K761186
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4630
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
National Biological Corp.
Date Received
December 6, 1976
Decision Date
February 28, 1977
Product Code
FTC
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FTC Light, Ultraviolet, Dermatological

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Other Clearances by National Biological Corp.

K Number Device Name
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
K904427 PANOSOL II UVB-206
K904426 PANOSOL II UVA-218
K904428 PANOSOL II UAB-228
K885029 HOUVA II UVA/UVB
Search all 27 clearances from National Biological Corp. →