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FDA 510(k)

MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400

K-Number: K983882 · 1999-03-15

ApplicantMicro-Medical Devices, Inc.
Decision Date1999-03-15
Product CodeHXR
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400 is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Medical Devices, Inc.. It received FDA 510(k) clearance on 1999-03-15 under 510(k) number K983882. The device is classified under product code HXR. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400?

MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400 is a medical device that received FDA 510(k) clearance on 1999-03-15. The listed applicant is Micro-Medical Devices, Inc.. The 510(k) number is K983882.

When did MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400 receive FDA 510(k) clearance?

MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400 received FDA 510(k) clearance on 1999-03-15, under 510(k) number K983882.

Who is the listed applicant for MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400?

The FDA 510(k) record lists Micro-Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400?

The FDA product code for MICRO ENDOSCOPE-STAINLESS STEEL, MODEL MMD-1300, MICRO ENDOSCOPE-POLYIMIDE,MODEL MMD-1400 is HXR.

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Other records listing Micro-Medical Devices, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K003695MICROSCOPE-STAINLESS STEEL/FIBER OPTIC: .5-2.6MM MODEL MMD 4500 SERIES AND 2.7-5.0MM MODEL MMD-4700 SERIESK963675THE FLAT PANEL STEIRLE DRAPE SYSTEM(TM), VIDEO MONITOR STERILE DRAPEK951482ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE)K951894ACCESS EXPANSION SYSTEMK945656THE COUPLER/DRAPE(TM), VIDEO CAMERA STERILE DRAPEK940141LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH

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Related Devices (Code: HXR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K873387VIDEO ARTHROSCOPE, 1.7MM X 55 MMArthropedics, Inc.K872281RAYLOR FUSION FUNNELCedar Surgical, Inc.K853436H-H HUNTER PASSIVE TENDON IMPLANTHolter-Hausner Intl.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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