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FDA 510(k)

X-VEE

K-Number: K810152 · 1981-03-17

ApplicantTemporaty Surgical Systems
Decision Date1981-03-17
Product CodeHKP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

X-VEE is the device name listed in this FDA 510(k) record. The listed applicant is Temporaty Surgical Systems. It received FDA 510(k) clearance on 1981-03-17 under 510(k) number K810152. The device is classified under product code HKP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-VEE?

X-VEE is a medical device that received FDA 510(k) clearance on 1981-03-17. The listed applicant is Temporaty Surgical Systems. The 510(k) number is K810152.

When did X-VEE receive FDA 510(k) clearance?

X-VEE received FDA 510(k) clearance on 1981-03-17, under 510(k) number K810152.

Who is the listed applicant for X-VEE?

The FDA 510(k) record lists Temporaty Surgical Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-VEE?

The FDA product code for X-VEE is HKP.

Related Devices (Code: HKP)

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.

K952558AARON VAC 2Aaron Medical IndustriesK950056THE GRIESHABER AXIAL CUTTERGrieshaber & Co.K950287UNIVIT PROBEMedical Instrument Development Laboratories, Inc.K896622VISITEC VITRECTOMY UNITVisitec Co.K890595MENTOR ANTERIOR SEGMENT VITRECTORMentor O & O, Inc.K832074CAVITRON/KELMAN PHACO-EMULSIFIER ASPIRACooperVision, 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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