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FDA 510(k)

VitroPRO

K-Number: K222052 · 2022-11-22

ApplicantCIVCO Medical Instruments Co., Inc.
Decision Date2022-11-22
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VitroPRO is the device name listed in this FDA 510(k) record. The listed applicant is CIVCO Medical Instruments Co., Inc.. It received FDA 510(k) clearance on 2022-11-22 under 510(k) number K222052. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VitroPRO?

VitroPRO is a medical device that received FDA 510(k) clearance on 2022-11-22. The listed applicant is CIVCO Medical Instruments Co., Inc.. The 510(k) number is K222052.

When did VitroPRO receive FDA 510(k) clearance?

VitroPRO received FDA 510(k) clearance on 2022-11-22, under 510(k) number K222052.

Who is the listed applicant for VitroPRO?

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

What is the FDA product code for VitroPRO?

The FDA product code for VitroPRO is ITX.

Other records listing CIVCO Medical Instruments Co., 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.

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Related Devices (Code: ITX)

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.

K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna Medical, Inc.K250883ULTRASONIC PROBE UM-3R (UM-3R); ULTRASONIC PROBE UM-G20-29R (UM-G20-29R)Olympus Medical Systems Corporation

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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