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FDA 510(k)

MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES

K-Number: K952323 · 1995-06-23

ApplicantMist, Inc.
Decision Date1995-06-23
Product CodeJOS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES is the device name listed in this FDA 510(k) record. The listed applicant is Mist, Inc.. It received FDA 510(k) clearance on 1995-06-23 under 510(k) number K952323. The device is classified under product code JOS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES?

MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES is a medical device that received FDA 510(k) clearance on 1995-06-23. The listed applicant is Mist, Inc.. The 510(k) number is K952323.

When did MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES receive FDA 510(k) clearance?

MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES received FDA 510(k) clearance on 1995-06-23, under 510(k) number K952323.

Who is the listed applicant for MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES?

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 ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES?

The FDA product code for MIST ELECTROSURGICAL PROBES, VARIOUS STYLES & SIZES is JOS.

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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 PROCEDURESK951648MIST ENDOSCOPIC NEEDLESK951481MIST ENDOSCOPIC CANNULASK951480MIST TROCARS

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Related Devices (Code: JOS)

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.

K161600Resection ElectrodesOlympus Winter & Ibe GmbHK050923LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATORConmed LinvatecK012684REPROCESSED ELECTROSURGICAL ELECTRODESterilmed, Inc.K011515MEDLINE GROUNDING PADMedline Industries, Inc.K003403ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999Highland / Marietta, Inc.K000333STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MODTriad Surgical Technologies, 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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