PERI-PUSHER

Accelerator, Linear, Medical

DIACOR, INC.

The following data is part of a premarket notification filed by Diacor, Inc. with the FDA for Peri-pusher.

Pre-market Notification Details

Device IDK953046
510k NumberK953046
Device Name:PERI-PUSHER
ClassificationAccelerator, Linear, Medical
Applicant DIACOR, INC. 3191 SOUTH 3300 EAST, SUITE 100-A Salt Lake City,  UT  84109
ContactGlenn N Waterman
CorrespondentGlenn N Waterman
DIACOR, INC. 3191 SOUTH 3300 EAST, SUITE 100-A Salt Lake City,  UT  84109
Product CodeIYE  
CFR Regulation Number892.5050 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-06-30
Decision Date1995-09-22

Trademark Results [PERI-PUSHER]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PERI-PUSHER
PERI-PUSHER
75116784 2055321 Dead/Cancelled
DIACOR, INC.
1996-06-10

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