FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DRTS REMOTE CONTROL DRAPE

K Number: K973067 · Decision Oct 16, 1997
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
14
Review Days
59

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Basic Information

Device Name
DRTS REMOTE CONTROL DRAPE
K Number
K973067
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Minrad, Inc.
Date Received
August 18, 1997
Decision Date
October 16, 1997
Product Code
JAA
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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K Number Device Name
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K062230 MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002
K041852 MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 310002
K041846 SABRESOURCE DRAPE
K021084 LIGHT SABER SPINAL NEEDLE
K013040 LIGHT SABER INTRODUCER NEEDLE
K982735 LIGHT SABER BONE BIOPSY NEEDLE
K982018 LIGHT SABER ASPIRATION NEEDLE
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