510(k) K831117
- Device
- MICROMAT W/VARIOUS MODELS
- Applicant
- PMT, Inc.
- 510(k) number
- K831117
- Product code
- FNW
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-05-30
- Date received
- 1983-04-05
- Regulation
- 878.4370
- Classification name
- Pad, Kelly
- Medical specialty
- General & Plastic Surgery
- Review panel
- General & Plastic Surgery
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- Carroll E Reynolds
- Address
- Box 464 Hopkins MN US 55343 55343
FDA Registration Numbers#
- 9680411
- 3008352964
- 3008808560
- 3014666579
- 3010373530
- 2182979
- 2183744
- 3013006775
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code FNW #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K841183 | SODIUM CHLORIDE SOLUTION BLOOD CELL | Reagent Laboratory, Inc. | 1984-05-21 |
Legacy Summary#
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FDA Review#
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