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
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Cleared under the same submission
K012492 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Red Oak Instruments, Llc
Sources (1)
- FDA UDI 50454c89-55c5-4079-8ff8-ce3cb042d6e6 36 fields · synced May 30, 2026