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

MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT

K Number: K864829 · Decision Jan 12, 1987
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
3
Review Days
34

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Basic Information

Device Name
MODEL NS-3CC NEURO-STIM PERIPHERAL NERVE STIMULAT
K Number
K864829
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Professional Instruments Co.
Date Received
December 9, 1986
Decision Date
January 12, 1987
Product Code
BXN
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
BXN Stimulator, Nerve, Battery-Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BXN), ordered by most recent decision date.

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Other Clearances by Professional Instruments Co.

K Number Device Name
K864830 TEFLON-COATED HYPODERMIC NEEDLES/REGIONAL BLOCK
K810206 DUAL TYPE ELECTRODE