FDA 510(k) Substantially Equivalent 🇺🇸 United States

COMFEEL PASTE

K Number: K840362 · Decision Nov 7, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
71
Review Days
286

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
COMFEEL PASTE
K Number
K840362
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Coloplast A/S
Date Received
January 26, 1984
Decision Date
November 7, 1984
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Other Clearances by Coloplast A/S

K Number Device Name
K221874 Altis Single Incision Sling System
K220420 Saffron Fixation System
K191536 Biatain Silicone Ag
K181811 ReTrace Ureteral Access Sheath
K173527 Digitex Delivery Device
K140310 Peristeen Anal Irrigation System
K150935 SpeediCath Compact Eve
K150927 Orchestra Hydrophilic Guidewire standard angled, Orchestra Hydrophilic Guidewire straight stiff, Orchestra Hydrophilic Guidewire angled stiff,Orchestra Hydrophilic Guidewire standard straight, Orchestra Hydrophilic Guidewire straight stiff
K143182 Speedicath Compact Male
K140523 RE-TRACE URETERAL ACCESS SHEATH, 12/14 CH/FR, LENGTH 35 CM, LENGTH 45 CM
Search all 71 clearances from Coloplast A/S →