FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OR TUBE RESTRAINT

K Number: K851874 · Decision Aug 8, 1985
Classifications
1
FEI Numbers
142
Registration Numbers
142
Same Product Code
46
Applicant Total
48
Review Days
101

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Basic Information

Device Name
OR TUBE RESTRAINT
K Number
K851874
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5770
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Kinetic Concepts, Inc.
Date Received
April 29, 1985
Decision Date
August 8, 1985
Product Code
CBH
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBH Device, Fixation, Tracheal Tube

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Other Clearances by Kinetic Concepts, Inc.

K Number Device Name
K050261 V.A.C. GRANUFOAM SILVER PROTECTION DRESSING
K041642 V.A.C. GRANUFOAM SILVER DRESSING
K032310 MINI V.A.C., V.A.C. FREEDOM, V.A.C. ATS
K022011 V.A.C. ABDOMINAL DRESSING
K021500 VACUUM ASSISTED CLOSURE
K021501 V.A.C. INSTILLAMAT (VACUUM ASSISTED CLOSURE INSTILLAMAT
K020781 WET CHAMBER
K992448 V.A.C. PLUS
K972176 HOME CARE BEAD BED
K972549 SIMPULSE
Search all 48 clearances from Kinetic Concepts, Inc. →