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FDA 510(k)

MODEL 6500 MERCURY ARC LIGHT SOURCE

K-Number: K896008 · 1989-12-27

ApplicantMedical Dynamics, Inc.
Decision Date1989-12-27
Product CodeGCP
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 6500 MERCURY ARC LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Dynamics, Inc.. It received FDA 510(k) clearance on 1989-12-27 under 510(k) number K896008. The device is classified under product code GCP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 6500 MERCURY ARC LIGHT SOURCE?

MODEL 6500 MERCURY ARC LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1989-12-27. The listed applicant is Medical Dynamics, Inc.. The 510(k) number is K896008.

When did MODEL 6500 MERCURY ARC LIGHT SOURCE receive FDA 510(k) clearance?

MODEL 6500 MERCURY ARC LIGHT SOURCE received FDA 510(k) clearance on 1989-12-27, under 510(k) number K896008.

Who is the listed applicant for MODEL 6500 MERCURY ARC LIGHT SOURCE?

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

What is the FDA product code for MODEL 6500 MERCURY ARC LIGHT SOURCE?

The FDA product code for MODEL 6500 MERCURY ARC LIGHT SOURCE is GCP.

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Other records listing Medical Dynamics, 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.

K974542TRUE VISION, TRUE VISION IIK921294VIDEO ENDOSCOPE-RIGID MODIFICATIONK934682SURGICAL VIDEO CAMERA AND ACCESSORIESK930568ADAIR/VERESS NEEDLE INTRODUCER SETK915538OVER THE WIRE STONE BASKETK914315OPTICAL CATHETER INTRODUCER SETS, MODIFICATION

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Related Devices (Code: GCP)

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.

K954614EOS BRAND DISPOSABLE PROCTOSCOPENorth Eos Industries, Inc.K896505PORGES UNIVERSAL HANDLESPorges Corp.K862424STEERABLE CATHETER SYSTEMEndovationsK860103MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVEEndotherapeuticsK843683MODULAR FIBERSCOPE SYSTEMReichert Scientific InstrumentsK833859TAMPONADE BALLOON CUFFAmerican Endoscopy, Inc.

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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