FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

MYOTEST DBS NERVE STIMULATOR

K Number: K890746 · Decision Jul 14, 1989
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
9
Review Days
151

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Basic Information

Device Name
MYOTEST DBS NERVE STIMULATOR
K Number
K890746
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Biometer Intl. A/S
Date Received
February 13, 1989
Decision Date
July 14, 1989
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 Biometer Intl. A/S

K Number Device Name
K925159 TOF-GUARD TRANSMISSION MONITOR
K914231 ELPHA 2000
K892396 MINI ACCELOGRAPH NEUROMUSCULAR TRANS. MONITOR
K893485 ACCELOGRAPH NEUROMUSCULAR TRANSMISSION MONITOR
K881196 AM 706 ELECTROMYOGRAPH, STIM., NEURO., EXTERNAL
K870619 ACCELOGRAPH
K860186 MYOTEST - NERVE STIMULATOR
K860187 MYOGRAPH 2000 - NEURO. TRANS. MONITOR & RECORDING