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

SAFE-STRIPS

K Number: K880548 · Decision Sep 29, 1988
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
2
Review Days
233

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Basic Information

Device Name
SAFE-STRIPS
K Number
K880548
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Medstar, Inc.
Date Received
February 9, 1988
Decision Date
September 29, 1988
Product Code
JOJ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
JOJ Indicator, Physical/Chemical Sterilization Process

Similar 510(k) Clearances

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Other Clearances by Medstar, Inc.

K Number Device Name
K921612 INTERTRON 4500, INTERTRON 5000, MASTERSTIM I-2