Identity
- Trade Name
- Vacuum Trap FDA UDI
- Generic Name
- General-purpose surgical suction system, vacuum FDA UDI
- Device Name
- PM9000 SERIES VAC TRAP FDA UDI
- Model / Reference
- PM9000 FDA UDI
- Description
- PM9000 SERIES VAC TRAP FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00855887006641 FDA UDI
- 510(k) Number
- K941818 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- General-purpose surgical suction system, vacuum FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: General-purpose surgical suction system, vacuum
Vacuum Trap by Precision Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General-purpose surgical suction system, vacuum.
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- Schuco — Allied Medical LLC · Class II
- ADULT TIP SUCKER HEX HANDLE WITH VENT — NOVOSCI CORP. · Class II
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Cleared under the same submission
K941818 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Precision Medical, Inc.
Sources (1)
- FDA UDI f4de21a8-600b-4884-a905-785ed35ea7bf 35 fields · synced May 31, 2026