Atlas FDA

DERMIDRESS

FDA 510(k) clearance K844463 · decided 1985-01-08

Clearance details

K-number
K844463
Device name
DERMIDRESS
Applicant
Kells Medical, Inc.
Decision
Substantially Equivalent
Date received
1984-11-20
Decision date
1985-01-08
Days to decision
49 days
Clearance type
Traditional
Product code
KGX
Device class
1
Regulation number
880.5240
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Burr Ridge, IL, US
Third-party review
No
Expedited review
No

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STERILE PLASTIC DRESSING (K944588)Smith & Nephew, Inc.1994-11-07
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BAND-AID(TM) BRAND ADHESIVE BANDAGE (K940536)Johnson & Johnson Consumer Products, Inc.1994-10-03
SHIPPERT PRESSURE BANDAGE (K940798)Denver Splint Co.1994-09-28
EMPI TAPE PATCHES (K941389)Empi1994-08-23

Recalls involving this device

No recalls on record reference this clearance.