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FDA 510(k)

WOM LAPAROFLATOR ELECTRONIC

K-Number: K921086 · 1992-04-07

ApplicantW.O.M. GmbH
Decision Date1992-04-07
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WOM LAPAROFLATOR ELECTRONIC is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. GmbH. It received FDA 510(k) clearance on 1992-04-07 under 510(k) number K921086. 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 WOM LAPAROFLATOR ELECTRONIC?

WOM LAPAROFLATOR ELECTRONIC is a medical device that received FDA 510(k) clearance on 1992-04-07. The listed applicant is W.O.M. GmbH. The 510(k) number is K921086.

When did WOM LAPAROFLATOR ELECTRONIC receive FDA 510(k) clearance?

WOM LAPAROFLATOR ELECTRONIC received FDA 510(k) clearance on 1992-04-07, under 510(k) number K921086.

Who is the listed applicant for WOM LAPAROFLATOR ELECTRONIC?

The FDA 510(k) record lists W.O.M. GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WOM LAPAROFLATOR ELECTRONIC?

The FDA product code for WOM LAPAROFLATOR ELECTRONIC is GCJ.

Related Clinical Trials

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.

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Other records listing W.O.M. GmbH 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.

K950035SURGIFLATOR 20K922632WOM HYSTEROFLATOR OP

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

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

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