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Micro Endoscope-Stainless Steel (Mmd-1300 +2 more)
FDA 510(k)Class I (US FDA 510(k))
510(k) K983882
Identifiers
- 510(k) Number
- K983882 FDA 510(k)
- FDA Product Code
- HXR FDA 510(k)
- Models / Variants
- Mmd-1300 FDA 510(k)Micro Endoscope-Polyimide FDA 510(k)Model Mmd-1400 FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 878.4800 FDA 510(k)
- Regulation Number
- 878.4800 FDA 510(k)
- Advisory Committee
- General, Plastic Surgery FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Micro Endoscope-Stainless Steel (Mmd-1300 +2 more) by Micro-Medical Devices, Inc. — Class I — FDA_510K — listed in FDA 510(k) — 3 models
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 | K983882 | Class I | Active |
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Manufacturer
- Manufacturer
- Micro-Medical Devices, Inc.
Sources (1)
- FDA 510(k) K983882 24 fields · synced Jun 18, 2026