SHARPX NEEDLE DESTRUCTION UNIT

FDA Premarket Approval P980015 S004

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval for labeling.

DeviceSHARPX NEEDLE DESTRUCTION UNIT
Generic NameSharps Needle Destruction Device
ApplicantINNOVATIVE MEDICAL SYSTEMS, INC.
Date Received2001-07-16
Decision Date2001-08-15
PMAP980015
SupplementS004
Product CodeMTV 
Advisory CommitteeGeneral Hospital
Supplement TypeSpecial (immediate Track)
Supplement ReasonLabeling Change - Indications/instructions/shelf Life/tradename
Expedited ReviewNo
Combination Product No
Applicant Address INNOVATIVE MEDICAL SYSTEMS, INC. 3610 Oakdale Drive mountain Brook, AL 35223

Supplemental Filings

Supplement NumberDateSupplement Type
P980015Original Filing
S005 2002-05-30 Real-time Process
S004 2001-07-16 Special (immediate Track)
S003 1999-09-14 Real-time Process
S002 1999-03-18 Real-time Process
S001 1998-12-08 Real-time Process

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