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FDA 510(k)

MICROSURGE THORACOSCOPIC INSTRUMENTS

K-Number: K955408 · 1996-01-31

ApplicantMicrosurge, Inc.
Decision Date1996-01-31
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MICROSURGE THORACOSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Microsurge, Inc.. It received FDA 510(k) clearance on 1996-01-31 under 510(k) number K955408. 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 MICROSURGE THORACOSCOPIC INSTRUMENTS?

MICROSURGE THORACOSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1996-01-31. The listed applicant is Microsurge, Inc.. The 510(k) number is K955408.

When did MICROSURGE THORACOSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

MICROSURGE THORACOSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1996-01-31, under 510(k) number K955408.

Who is the listed applicant for MICROSURGE THORACOSCOPIC INSTRUMENTS?

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

What is the FDA product code for MICROSURGE THORACOSCOPIC INSTRUMENTS?

The FDA product code for MICROSURGE THORACOSCOPIC INSTRUMENTS is GCJ.

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Other records listing Microsurge, 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.

K964109MICROSURGE LAPAROSCOPIC PERMACLIP CARTRIDGE WITH IMPLANTABLE CLIPK960554DETACHATIP THORACOSCOPIC SCISSORSK954641ENDO-LEADERK954072MICROSURGE PUNCTURE CLOSE DEVICEK954520MICROSURGE VERESS NEEDLEK953121MICROSURGE THORACOSCOPIC ACCESS 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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