Identity
- Trade Name
- KOWA Applanation Tonometer HA-2 FDA UDI
- Generic Name
- Ophthalmic tonometer, battery-operated FDA UDI
- Device Name
- For the measurement of intraocular pressure in the diagnosis of glaucoma. FDA UDI
- Model / Reference
- ATO-6K FDA UDI
- Description
- For the measurement of intraocular pressure in the diagnosis of glaucoma. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04987646803799 FDA UDI
- 510(k) Number
- K960924 FDA UDI
- FDA Product Code
- HKY FDA UDI
- GMDN Term
- Ophthalmic tonometer, battery-operated FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1930 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
Yes
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
Dimensions & Sizes
- Size
- Weight — 240 Gram FDA UDILength — 290 Millimeter FDA UDI
Category: Ophthalmic tonometer, battery-operated
KOWA Applanation Tonometer HA-2 by Kowa Co. , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Kowa Co. , Ltd.
Sources (1)
- FDA UDI 746f17df-6224-41e0-afdf-1c8367fb320e 36 fields · synced Jun 8, 2026