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FDA 510(k)

SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM

K-Number: K942740 · 1994-08-23

ApplicantSharplan Lasers, Inc.
Decision Date1994-08-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sharplan Lasers, Inc.. It received FDA 510(k) clearance on 1994-08-23 under 510(k) number K942740. 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 SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM?

SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Sharplan Lasers, Inc.. The 510(k) number is K942740.

When did SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM receive FDA 510(k) clearance?

SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM received FDA 510(k) clearance on 1994-08-23, under 510(k) number K942740.

Who is the listed applicant for SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM?

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

What is the FDA product code for SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM?

The FDA product code for SHARPLAN-CONTEC EC-1000 ENDOSCOPY VIDEO CAMERA SYSTEM is GCJ.

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Other records listing Sharplan Lasers, 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.

K973354SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000)K972099SHARPLAN EPITOUCH RUBY LASER SYSTEMK971874SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000)K971648SHARPLAN ERBIUM: YAG LASER (4020)K971743SHARPLAN CO2 SURGICAL LASER SYSTEMK962446SHARPLAN RUBY LASER SYSTEM

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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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