Atlas FDA

BINDAFIX

FDA 510(k) clearance K791211 · decided 1979-08-03

Clearance details

K-number
K791211
Device name
BINDAFIX
Applicant
Conphar, Inc.
Decision
Substantially Equivalent
Date received
1979-07-02
Decision date
1979-08-03
Days to decision
32 days
Clearance type
Traditional
Product code
FQM
Device class
1
Regulation number
880.5075
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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RecordFirmDate
PETIT SILMA ELASTIC BANDAGE WITH GERMANIUM/TITANIUM OXIDE (K040936)Leda Co., Ltd.2004-05-03
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SKIN SAVER SYSTEMS (K952738)Skin Saver Systems, Inc.1995-09-29
ASPEN ESMARK BANDAGE (K872868)Aspen Laboratories, Inc.1987-07-31
TUBE-BANDAGE FOR HUMAN DIGITS 200 (K840107)Zens Health Care Products1984-04-25
MEDICALEX (K831728)Medicalex1984-01-09
ORTHO WRAP (K830622)Fast Wrap Co., Inc.1983-06-20
COMPRESSOGRIP TUBULAR ELASTIC BANDAGE (K831551)Fred Sammons, Inc.1983-06-07
BIAS STOCKINETTE (K820141)Stan-Pak Ent.1982-02-05
TUBULAR STOCKINETTE (K820142)Stan-Pak Ent.1982-02-05
ELASTIC BANDAGE (K820094)Stan-Pak Ent.1982-01-29

Recalls involving this device

No recalls on record reference this clearance.