← Back to catalogue

Precision Medical

FDA UDI

Class II (US FDA UDI)

by Precision Medical, Inc.

Identity

Trade Name
Precision Medical FDA UDI
Generic Name
General-purpose surgical suction system, vacuum FDA UDI
Device Name
VAC TRAP,FILTERED FDA UDI
Model / Reference
PMX900 SERIES FDA UDI
Description
VAC TRAP,FILTERED FDA UDI

Identifiers

Catalog Number
PMX900 FDA UDI
Primary DI / UDI-DI
00850027043739 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

Yes

FDA UDI

Category: General-purpose surgical suction system, vacuum

Precision Medical 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.

Cleared under the same submission

K941818 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Precision Medical, Inc.

Sources (1)

  • FDA UDI a2dd0fbc-1918-4102-a8ff-d11bb88d3b40 35 fields · synced May 29, 2026