← Back to catalogue

Summit

FDA UDI

Class II (US FDA UDI)

by Harmar Summit, LLC

Identity

Trade Name
SUMMIT FDA UDI
Generic Name
Stairlift, chair FDA UDI
Device Name
ASS'Y, CHASSIS, DC - WARRANTY FDA UDI
Model / Reference
SL350 FDA UDI
Description
ASS'Y, CHASSIS, DC - WARRANTY FDA UDI

Identifiers

Catalog Number
17164-W FDA UDI
Primary DI / UDI-DI
00817650022715 FDA UDI
510(k) Number
K032880 FDA UDI
FDA Product Code
ILK FDA UDI
GMDN Term
Stairlift, chair FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5150 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

Yes

FDA UDI

Category: Stairlift, chair

Summit by Harmar Summit, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stairlift, chair.

Cleared under the same submission

K032880 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
Harmar Summit, LLC

Sources (1)

  • FDA UDI f2276a2c-c612-4233-99f1-0e72f4d4264b 36 fields · synced May 30, 2026