FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DACOMED EXTERNAL MALE CONTINENCE DEVICE

K Number: K885323 · Decision Feb 8, 1989
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
10
Applicant Total
20
Review Days
42

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Basic Information

Device Name
DACOMED EXTERNAL MALE CONTINENCE DEVICE
K Number
K885323
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5160
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Dacomed Corp.
Date Received
December 28, 1988
Decision Date
February 8, 1989
Product Code
FHA
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FHA Clamp, Penile

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Other Clearances by Dacomed Corp.

K Number Device Name
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K920409 DACOMED BATTERY OPERATED VACUUM ERECTION DEVICE
K920420 DURA II PENILE PROSTHESIS
K912344 MODIFIED DURAPHASE(TM) IMPLANTED PENILE PROSTHESIS
K900774 DACOMED NEGATIVE PRESSURE ERECTION DEVICE
K880391 DACOMED CYSTOMETER
K871653 DURAPHASE PENILE PROSTHESIS
K870320 DACOMED PENILE PROSTHESIS SIZER
K854118 DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS
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