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

I.M PROBES

K Number: K802951 · Decision Dec 17, 1980
Classifications
1
FEI Numbers
373
Registration Numbers
373
Same Product Code
14
Applicant Total
26
Review Days
27

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Basic Information

Device Name
I.M PROBES
K Number
K802951
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Hogan & Hartson
Date Received
November 20, 1980
Decision Date
December 17, 1980
Product Code
HXB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HXB Probe

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