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

SPORICIDIN BRAND DISINFECTANT SPRAY

K Number: K904580 · Decision May 18, 1992
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
72
Applicant Total
8
Review Days
587

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Basic Information

Device Name
SPORICIDIN BRAND DISINFECTANT SPRAY
K Number
K904580
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6890
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Sporicidin Intl.
Date Received
October 9, 1990
Decision Date
May 18, 1992
Product Code
LRJ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LRJ Disinfectant, Medical Devices

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LRJ), ordered by most recent decision date.

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Other Clearances by Sporicidin Intl.

K Number Device Name
K003087 MODIFICATION TO SPORICIDIN STERILIZING AND DISINFECTING SOLUTION
K983194 SPORICIDIN STERILIZING AND DISINFECTING SOLUTION (SSDS)
K926013 SPORICIDIN BRAND DISINFECT TOWEL, SPRAY/SOLUT MODI
K922262 SPORICIDIN BRAND DISINFECT TOWELETTES/SPRAY/SOLUT
K904581 SPORICIDIN BRAND DISINFECTANT SOLUTION
K904579 SPORICIDIN BRAND DISINFECTANT TOWELETTES
K830722 SPORIDIDIN-D COLD STERILIZING/SOLUTION