510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K983882Substantially Equivalent

Micro Endoscope-Stainless Steel, Model Mmd-1300, Micro Endoscope-Polyimide,model Mmd-1400

Micro Medical Devices, Inc., Cleveland OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K983882 is the FDA 510(k) clearance record for MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400, a class I device, cleared for Micro-Medical Devices, Inc. on under FDA product code HXR (Spatula, Orthopedic). FDA records list 8 510(k) clearances for Micro-Medical Devices, Inc., from to . As of , FDA records show no recalls naming K983882.

Clearance record

Decision date
Received
(133 days to decision)
Product code
HXR Spatula, Orthopedic
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Micro-Medical Devices, Inc. 11000 Cedar Ave., Cleveland OH
510(k) summary
Summary
Third party review
No

Clearances, product code HXR

Trailing 12 months

FDA records hold no clearances under product code HXR in the trailing twelve months.

FDA records show no clearances under product code HXR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HXR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260