FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

RAPIDO-LASTIC IN STERILE FORM

K Number: K821701 · Decision Jul 22, 1982
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
270
Applicant Total
12
Review Days
44

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Basic Information

Device Name
RAPIDO-LASTIC IN STERILE FORM
K Number
K821701
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Conco Medical Co.
Date Received
June 8, 1982
Decision Date
July 22, 1982
Product Code
EFQ
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
EFQ Gauze/Sponge, Internal

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Other Clearances by Conco Medical Co.

K Number Device Name
K904819 SHUR-LOCK ICE WRAP SYSTEM
K820826 STAX FINGER SPLINT
K820381 FINGER PROTECTOR
K820382 FROG SPLINT
K820380 CURVED FINGER SPLINT
K820383 FINGER COT
K760139 BANDAGE, E-COTTON ELASTIC
K760138 BANDAGE, CEB COTTON ELASTIC
K760140 BANDAGE, WRINKY-LASTIC ELASTIC GAUZE
K760142 BANDAGE, RAPIDO-LASTIC COTTON/NYLON
Search all 12 clearances from Conco Medical Co. →