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FDA 510(k)

MAHE INSTRUMENTS

K-Number: K935442 · 1994-03-14

ApplicantMahe-Medizintechnik
Decision Date1994-03-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAHE INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Mahe-Medizintechnik. It received FDA 510(k) clearance on 1994-03-14 under 510(k) number K935442. 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 MAHE INSTRUMENTS?

MAHE INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-03-14. The listed applicant is Mahe-Medizintechnik. The 510(k) number is K935442.

When did MAHE INSTRUMENTS receive FDA 510(k) clearance?

MAHE INSTRUMENTS received FDA 510(k) clearance on 1994-03-14, under 510(k) number K935442.

Who is the listed applicant for MAHE INSTRUMENTS?

The FDA 510(k) record lists Mahe-Medizintechnik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAHE INSTRUMENTS?

The FDA product code for MAHE INSTRUMENTS is GCJ.

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Other records listing Mahe-Medizintechnik 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.

K942821MAHE INSTRUMENTSK942819TROCAR WITH SHIELDK933768COAGULATOR, LAPAROSCOPIC, LUNIPOLAR/ACCESSORIESK933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYK933770FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPEK933772PUNCH SURGICAL

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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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