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FDA 510(k)

VASCULAR LABORATORY TREADMILL VT1

K-Number: K833588 · 1983-11-14

Decision Date1983-11-14
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VASCULAR LABORATORY TREADMILL VT1 is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K833588. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR LABORATORY TREADMILL VT1?

VASCULAR LABORATORY TREADMILL VT1 is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Medasonics, Inc.. The 510(k) number is K833588.

When did VASCULAR LABORATORY TREADMILL VT1 receive FDA 510(k) clearance?

VASCULAR LABORATORY TREADMILL VT1 received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833588.

Who is the listed applicant for VASCULAR LABORATORY TREADMILL VT1?

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

What is the FDA product code for VASCULAR LABORATORY TREADMILL VT1?

The FDA product code for VASCULAR LABORATORY TREADMILL VT1 is IOL.

Related Clinical Trials

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.

Other records listing Medasonics, 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.

View all 19 devices →

Related Devices (Code: IOL)

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.

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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