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FDA 510(k)

RMI SURGICCAL SITE VISUALIZATION WAND

K-Number: K922083 · 1993-01-29

ApplicantResearch Medical, Inc.
Decision Date1993-01-29
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RMI SURGICCAL SITE VISUALIZATION WAND is the device name listed in this FDA 510(k) record. The listed applicant is Research Medical, Inc.. It received FDA 510(k) clearance on 1993-01-29 under 510(k) number K922083. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMI SURGICCAL SITE VISUALIZATION WAND?

RMI SURGICCAL SITE VISUALIZATION WAND is a medical device that received FDA 510(k) clearance on 1993-01-29. The listed applicant is Research Medical, Inc.. The 510(k) number is K922083.

When did RMI SURGICCAL SITE VISUALIZATION WAND receive FDA 510(k) clearance?

RMI SURGICCAL SITE VISUALIZATION WAND received FDA 510(k) clearance on 1993-01-29, under 510(k) number K922083.

Who is the listed applicant for RMI SURGICCAL SITE VISUALIZATION WAND?

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

What is the FDA product code for RMI SURGICCAL SITE VISUALIZATION WAND?

The FDA product code for RMI SURGICCAL SITE VISUALIZATION WAND is FQH.

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Other records listing Research Medical, 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.

K970739RMI HEMOCONCENTRATOR PREFERENCE PACKK964833RMI DUAL FLUID IRRIGATING SYRINGEK961927RMI HEMOCONCENTRACTOR TUBING SETK960098RMI INTERNAL MAMMARY ARTERY CANNULAK951344RMI HEMOCONCENTRATORK920936RMI EXTERNAL CORONARY ARTERY OCCLUDER

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Related Devices (Code: FQH)

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.

K253996BD Surgiphor™ Antimicrobial Irrigation System (910110)Becton, Dickinson and Company (BD)K253445BD Surgiphor™ 1000 mL Antimicrobial Irrigation System (910120)BdK231023ERBEJET® 2 SystemErbe Elektromedizin GmbHK220759Armis VeriCyn Wound WashArmis Biopharma, Inc.K220964VERSAJET Hydrosurgery System (III)Smith & Nephew Medical LimitedK221504BD Surgiphor™ Antimicrobial Irrigation SystemBd

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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