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APG Air-Plethysmograph

FDA UDI

Class II (US FDA UDI)

by Aci Medical, Llc

Identity

Trade Name
APG Air-Plethysmograph FDA UDI
Generic Name
Limb plethysmograph FDA UDI
Device Name
Pneumatic plethysmograph. FDA UDI
Model / Reference
APG-1000 FDA UDI
Description
Pneumatic plethysmograph. FDA UDI

Identifiers

Catalog Number
APG-1000 FDA UDI
Primary DI / UDI-DI
00860446000312 FDA UDI
510(k) Number
K881291 FDA UDI
FDA Product Code
JOM FDA UDI
GMDN Term
Limb plethysmograph FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2780 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

No

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: Limb plethysmograph

APG Air-Plethysmograph by Aci Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limb plethysmograph.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aci Medical, Llc

Sources (1)

  • FDA UDI 425f2d88-00a7-4632-9891-a19ff29ff9f9 36 fields · synced May 30, 2026