← Back to catalogue

Precision Medical Inc.

FDA UDI

Class II (US FDA UDI)

by Precision Medical, Inc.

Identity

Trade Name
Precision Medical Inc. FDA UDI
Generic Name
Vacuum suction regulator/regulation set, general-purpose FDA UDI
Device Name
PM3300 SERIES,VAC REG,INTERMITTENT,300MMHG,DIGITAL,BEACON MEDAES FDA UDI
Model / Reference
PM3300 FDA UDI
Description
PM3300 SERIES,VAC REG,INTERMITTENT,300MMHG,DIGITAL,BEACON MEDAES FDA UDI

Identifiers

Primary DI / UDI-DI
00855887006474 FDA UDI
510(k) Number
K944479 FDA UDI
FDA Product Code
KDP FDA UDI
GMDN Term
Vacuum suction regulator/regulation set, general-purpose 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vacuum suction regulator/regulation set, general-purpose

Precision Medical Inc. by Precision Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum suction regulator/regulation set, general-purpose.

Cleared under the same submission

K944479 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 d1ffc657-3ba7-4559-a276-2012caa94d93 35 fields · synced May 30, 2026