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

PODIATRIC MATERIAL

K Number: K780391 · Decision Jun 14, 1978
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
1
Applicant Total
18
Review Days
96

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Basic Information

Device Name
PODIATRIC MATERIAL
K Number
K780391
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Crown Delta Corp.
Date Received
March 10, 1978
Decision Date
June 14, 1978
Product Code
MNE
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
MNE Orthosis, Moldable, Supportive, Skin Protective

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K940132 PODIATRIC MATERIAL
K930248 VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM
K926150 VINYL ADDITION SILICONE SYSTEM
K901991 SILICONE ELASTOMER PUTTY
K901990 VINYL SILICONE ELASTOMER MATERIAL
K872745 VINYL POLYSILOXANE IMPRESSION SYSTEM
K871409 VINYL POLYSILOXANE IMPRESSION SYSTEM
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