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

CALIBRATED TISSUE GRAFT PRESS

K Number: K822368 · Decision Sep 9, 1982
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
0
Applicant Total
80
Review Days
34

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Basic Information

Device Name
CALIBRATED TISSUE GRAFT PRESS
K Number
K822368
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4420
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Treace Medical, Inc.
Date Received
August 6, 1982
Decision Date
September 9, 1982
Product Code
JYW
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
JYW Press, Vein

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K872000 EYE GARD
K870765 CANNULATED INSTRUMENT CLEANERS
K871706 OPTHA PREP
K870759 CLEANING SOLUTION, CATALOG NO. 8203
K870766 PROSTHESIS WIRE
K870760 BUR BRUSH
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