FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MICROLET FAMILY OF NEEDLE/DEPTH ELECT-
K Number: K802249
·
Decision Nov 19, 1980
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
57
Applicant Total
17
Review Days
64
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Basic Information
- Device Name
- MICROLET FAMILY OF NEEDLE/DEPTH ELECT-
- K Number
- K802249
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.1330
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Progress Mankind Technology
- Date Received
- September 16, 1980
- Decision Date
- November 19, 1980
- Product Code
- GZL
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| GZL | Electrode, Depth | FDA class 2 | Neurology |
Similar 510(k) Clearances
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Other Clearances by Progress Mankind Technology
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|---|---|---|---|
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| K871663 | PMT TRACTION TONGS | Jun 19, 1987 | Substantially Equivalent |
| K854157 | PMT ACCUPRESSURE INFUSION SYSTEM 3601 | Feb 13, 1986 | Substantially Equivalent |
| K845035 | ELECTRODE FOR NEUROLOGICAL SURGERY 2111 | Jul 30, 1985 | Substantially Equivalent for Some Indications |
| K845036 | TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 | Jun 26, 1985 | Substantially Equivalent |
| K834047 | PMT-HALO/ORTHOPEDIC JACKET SYSTEM | Feb 17, 1984 | Substantially Equivalent |
| K831329 | PMT VAXIOM STEREOTACTIC SYS #FX001 | Jun 15, 1983 | Substantially Equivalent |
| K830530 | TEMP TRACE | Apr 6, 1983 | Substantially Equivalent |
| K812744 | LEVY BIOTAC #LX001 BIOPSY PROBE HOLDER | Dec 3, 1981 | Substantially Equivalent |