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

E.T. STRAP #6000

K Number: K830706 · Decision Apr 28, 1983
Classifications
1
FEI Numbers
142
Registration Numbers
142
Same Product Code
46
Applicant Total
1
Review Days
52

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Basic Information

Device Name
E.T. STRAP #6000
K Number
K830706
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5770
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Rnd Medical Products, Inc.
Date Received
March 7, 1983
Decision Date
April 28, 1983
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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