FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NEUROMUSCULAR TRANSMISSION MONITOR
K Number: K905092
·
Decision Jun 25, 1991
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
38
Review Days
223
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Basic Information
- Device Name
- NEUROMUSCULAR TRANSMISSION MONITOR
- K Number
- K905092
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.2775
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Utah Medical Products, Inc.
- Date Received
- November 14, 1990
- Decision Date
- June 25, 1991
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| BXN | Stimulator, Nerve, Battery-Powered | FDA class 2 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (BXN), ordered by most recent decision date.
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MiniStim MS-IVB Peripheral Nerve Stimulator
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STIMPOD ST2-3010 NERVE STIMULATOR
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EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTIN
FDA 510(k)
FDA Class 2
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