Microscope-Stainless Steel/fiber Optic: .5-2.6Mm Model Mmd 4500 Series and 2.7-5.0Mm Model Mmd-4700 Series
K003695 is the FDA 510(k) clearance record for MICROSCOPE-STAINLESS STEEL/FIBER OPTIC: .5-2.6MM MODEL MMD 4500 SERIES AND 2.7-5.0MM MODEL MMD-4700 SERIES, a class II device, cleared for Micro-Medical Devices, Inc. on under FDA product code HRX (Arthroscope). FDA's definition for product code HRX reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 8 510(k) clearances for Micro-Medical Devices, Inc., from to . As of , FDA records show no recalls naming K003695.
Clearance record
- Decision date
- Received
- (76 days to decision)
- Product code
- HRX Arthroscope
- Regulation
- 21 CFR 888.1100
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Micro-Medical Devices, Inc. 11000 Cedar Ave., Cleveland OH
- 510(k) summary
- Summary
- Third party review
- No
Clearances, product code HRX
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 2 |
| December 2025 | 2 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 1 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 2 |
| September 2026 | 0 |
| October 2026 | 0 |
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