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Sr-3053

FDA UDI

Class II (US FDA UDI)

by Red Oak Instruments, Llc

Identity

Trade Name
SR-3053 FDA UDI
Generic Name
Hand dynamometer/pinchmeter, electronic FDA UDI
Device Name
Fine motor control measurements FDA UDI
Model / Reference
S FDA UDI
Description
Fine motor control measurements FDA UDI

Identifiers

Catalog Number
SR-3053-S FDA UDI
Primary DI / UDI-DI
B824SR3053S1 FDA UDI
510(k) Number
K012492 FDA UDI
FDA Product Code
LBB FDA UDI
GMDN Term
Hand dynamometer/pinchmeter, electronic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1240 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand dynamometer/pinchmeter, electronic

Sr-3053 by Red Oak Instruments, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand dynamometer/pinchmeter, electronic.

Cleared under the same submission

K012492 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 50454c89-55c5-4079-8ff8-ce3cb042d6e6 36 fields · synced May 30, 2026