← Back to catalogue

PFT Kit B

FDA UDI

Class II (US FDA UDI)

by A-M Systems, Inc.

Identity

Trade Name
PFT Kit B FDA UDI
Generic Name
Pulmonary function testing kit FDA UDI
Device Name
PFT Kit B, 35mm Pulmonary Function Kit - Case FDA UDI
Model / Reference
PFT Kit B - 180052 FDA UDI
Description
PFT Kit B, 35mm Pulmonary Function Kit - Case FDA UDI

Identifiers

Catalog Number
180052 FDA UDI
Primary DI / UDI-DI
00817081021226 FDA UDI
510(k) Number
K000654 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Pulmonary function testing kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Pulmonary function testing kit

PFT Kit B by A-M Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function testing kit.

Cleared under the same submission

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
A-M Systems, Inc.

Sources (1)

  • FDA UDI bb044a15-fc07-414c-89ba-6471ae3209e3 36 fields · synced May 30, 2026