ProView Plus PM1318
ProView Plus PM1318 (PM1318-1) is a Class II device made by MicroCare, LLC, cleared under FDA 510(k) K953829 on 9 Nov 1995 and listed in FDA GUDID since 26 Oct 2022 (UDI-DI H816MPM13181), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberH816MPM13181 | Date26 Oct 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK953829 | Date9 Nov 1995 | StatusActive |
Official records
- FDA 510(k) database K953829
Across registries
- FDA 510(k) K953829 decided 9 Nov 1995 Active
- FDA GUDID UDI-DI H816MPM13181 listed 26 Oct 2022 Listed
Timeline
- Cleared FDA 510(k) K953829
- Listed FDA GUDID H816MPM13181
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- ProView Plus
- Generic name
- Sterilization packaging, single-use
- Model / Ref / Catalog
- PM1318, PM1318-1
- Primary DI / UDI-DI
- H816MPM13181
- FDA product code
- KCT
- GMDN term
- Sterilization packaging, single-use
- Device class
- Class II
- Regulation number
- 880.6850
- GUDID distribution status
- In Commercial Distribution
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