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FDA 510(k)

MIST ENDOSCOPIC PROBES

K-Number: K951692 · 1995-05-03

ApplicantMist, Inc.
Decision Date1995-05-03
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MIST ENDOSCOPIC PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Mist, Inc.. It received FDA 510(k) clearance on 1995-05-03 under 510(k) number K951692. 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 MIST ENDOSCOPIC PROBES?

MIST ENDOSCOPIC PROBES is a medical device that received FDA 510(k) clearance on 1995-05-03. The listed applicant is Mist, Inc.. The 510(k) number is K951692.

When did MIST ENDOSCOPIC PROBES receive FDA 510(k) clearance?

MIST ENDOSCOPIC PROBES received FDA 510(k) clearance on 1995-05-03, under 510(k) number K951692.

Who is the listed applicant for MIST ENDOSCOPIC PROBES?

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

What is the FDA product code for MIST ENDOSCOPIC PROBES?

The FDA product code for MIST ENDOSCOPIC PROBES is GCJ.

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Other records listing Mist, 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.

K970937MIST MICRO INTERCHANGEABLE SCOPE SYSTEM (TM)K971150MIST PANORAMIC LAPAROSCOPE A RIGID LAPAROSCOPEK952290MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES, SURGICAL INSTRUMENTS USED DURING ENDOSCOPIC PROCEDURESK952323MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZESK951648MIST ENDOSCOPIC NEEDLESK951480MIST TROCARS

View all 8 devices →

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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