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

PROTECT-O-SEAL

K Number: K813014 · Decision Nov 10, 1981
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
264
Applicant Total
29
Review Days
14

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Basic Information

Device Name
PROTECT-O-SEAL
K Number
K813014
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.2800
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Tri-Med, Inc.
Date Received
October 27, 1981
Decision Date
November 10, 1981
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

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K961863 PARACENTESIS TRAYS
K875224 HUDSON CRANINAL BURRS
K850747 TRI-MED MODEL 105 SPECIAL AIRWAY ADAPTOR
K850746 TRI-MED MODEL 126 SAMPLE LINE W/EXTENDED LIFE NAFI
K850745 TRI-MED MODEL 112 MOISTURE TRAP
K843681 RESPIRATION & HEART RATE MONITOR 530
K843285 TRI-MED 610 CAPNOSTAT GAS ANALYZER
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