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FDA 510(k)

VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01

K-Number: K102626 · 2010-11-12

ApplicantVega Technologies, Inc.
Decision Date2010-11-12
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01 is the device name listed in this FDA 510(k) record. The listed applicant is Vega Technologies, Inc.. It received FDA 510(k) clearance on 2010-11-12 under 510(k) number K102626. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01?

VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01 is a medical device that received FDA 510(k) clearance on 2010-11-12. The listed applicant is Vega Technologies, Inc.. The 510(k) number is K102626.

When did VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01 receive FDA 510(k) clearance?

VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01 received FDA 510(k) clearance on 2010-11-12, under 510(k) number K102626.

Who is the listed applicant for VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01?

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

What is the FDA product code for VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01?

The FDA product code for VEGA MEDICAL SUCTION EQUIPMENT, MODEL SU-01/SU-DC01 is JCX.

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Other records listing Vega Technologies, 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.

K102625VEGA CPAP SYSTEM/HEATED HUMIDIFIER, MODEL CP-03K102934INFRARED EAR THERMOMETER, MODEL IR-04MTK041516DIGITAL THERMOMETER, MODELS MT-XX8 AND MT-XX9K031413VIGORMIST COMPRESSOR NEBULIZERK002831VEGA ULTRASONIC NEBULIZER

Related Devices (Code: JCX)

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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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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