← Back to catalogue
Slit Lamp Sl-D701
FDA UDIFDA 510(k)Class II (US FDA UDI)
510(k) K133667
by Topcon Corp.
Identity
- Trade Name
- SLIT LAMP SL-D701 FDA UDI
- Generic Name
- Ophthalmic examination slit lamp FDA UDI
- Model / Reference
- SL-D701 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04562123288285 FDA UDI
- FDA Product Code
- HJO FDA UDI
- GMDN Term
- Ophthalmic examination slit lamp FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.1850 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
Yes
FDA UDI
Category: Ophthalmic examination slit lamp
Slit Lamp Sl-D701 by Topcon Corp. — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic examination slit lamp.
- Mediworks — SHANGHAI MEDIWORKS PRECISION INSTRUMENTS CO., LTD. · Class II
- ILLUMINIX — Illuminix Industries LLC · Class II
- Visionix — RIGHT MFG. CO., LTD. · Class II
- Slit Lamp BQ 900 — Haag-Streit AG · Class II
- S4 OPTIK — COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL · Class II
- SLH 5XC 6V TBL USA — KEELER LIMITED · Class II
- SLH 5XC 6V TBL — KEELER LIMITED · Class II
- Eli Ezer — U.S. OPHTHALMIC, L.L.C. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K133667 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Topcon Corp.
Sources (2)
- FDA UDI 2495009a-f75e-49c5-8f36-bd8b2e1a9f8b 56 fields · synced Jun 18, 2026
- FDA 510(k) K133667 1 fields · synced Jun 4, 2026