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FDA 510(k)

MEDICAM ENDOCOUPLER AND BEAMSPLITTER

K-Number: K941693 · 1994-06-27

ApplicantM.P. Video, Inc.
Decision Date1994-06-27
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDICAM ENDOCOUPLER AND BEAMSPLITTER is the device name listed in this FDA 510(k) record. The listed applicant is M.P. Video, Inc.. It received FDA 510(k) clearance on 1994-06-27 under 510(k) number K941693. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAM ENDOCOUPLER AND BEAMSPLITTER?

MEDICAM ENDOCOUPLER AND BEAMSPLITTER is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is M.P. Video, Inc.. The 510(k) number is K941693.

When did MEDICAM ENDOCOUPLER AND BEAMSPLITTER receive FDA 510(k) clearance?

MEDICAM ENDOCOUPLER AND BEAMSPLITTER received FDA 510(k) clearance on 1994-06-27, under 510(k) number K941693.

Who is the listed applicant for MEDICAM ENDOCOUPLER AND BEAMSPLITTER?

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

What is the FDA product code for MEDICAM ENDOCOUPLER AND BEAMSPLITTER?

The FDA product code for MEDICAM ENDOCOUPLER AND BEAMSPLITTER is GCJ.

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Other records listing M.P. Video, 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.

K951386COMBINATION CAMERA/LIGHT SOURCEK943342MEDICAM XENON LIGHT SOURCEK942358AUTOCLAVEABLE MEDICAM 900 DIGICON CAMERAK941773MEDICAM 900 REMOTEK893828ML-800 AUTOELECTRONIC LIGHT SOURCEK882924MEDICAM MC-7 AND RP-7 SURGICAL CAMERAS

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Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.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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