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FDA 510(k)

VTI DISPOSABLE PRESSURE DISPLAY SET

K-Number: K944764 · 1994-12-27

ApplicantVascular Technology Incorporated
Decision Date1994-12-27
Product CodeDXS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VTI DISPOSABLE PRESSURE DISPLAY SET is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Technology Incorporated. It received FDA 510(k) clearance on 1994-12-27 under 510(k) number K944764. The device is classified under product code DXS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VTI DISPOSABLE PRESSURE DISPLAY SET?

VTI DISPOSABLE PRESSURE DISPLAY SET is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is Vascular Technology Incorporated. The 510(k) number is K944764.

When did VTI DISPOSABLE PRESSURE DISPLAY SET receive FDA 510(k) clearance?

VTI DISPOSABLE PRESSURE DISPLAY SET received FDA 510(k) clearance on 1994-12-27, under 510(k) number K944764.

Who is the listed applicant for VTI DISPOSABLE PRESSURE DISPLAY SET?

The FDA 510(k) record lists Vascular Technology Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VTI DISPOSABLE PRESSURE DISPLAY SET?

The FDA product code for VTI DISPOSABLE PRESSURE DISPLAY SET is DXS.

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Other records listing Vascular Technology Incorporated 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.

K082870VTI INTRAOPERATIVE DOPPLER SYSTEMSK031091VTI 20 MHZ GATED DOPPLERK002990VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001K922738VTI OXYGEN ANALYZERK890058VASCULAR TECHNOLOGY UNIOX OXYGEN ALARMK883960GIPHY MONITOR

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Related Devices (Code: DXS)

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.

K113235PRESSURE DISPLAY BOX,DLP DISPOSABLE PRESSURE DISPLAY SETS-NON STERILE VERSIONSMedtronic, Inc.K912045TMP PRESSURE ISOLATORR, TMP PRESSURE MONITOR SYSTLifestream Int'L, Inc.K900797STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XRShiley, Inc.K873802PRESSURE BARRIER KIT CAT. NO. PBK-3American Omni Medical, Inc.K862836STOCKERT-SHILEY CAPS AND CAPS DUAL PRESSURE MODULEShiley, Inc.K852232PRESSURE DISPLAY BOX #60000/TUBING SET #61000Dlp, 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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