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FDA 510(k)

MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED)

K-Number: K900720 · 1990-11-05

Decision Date1990-11-05
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED) is the device name listed in this FDA 510(k) record. The listed applicant is Mortara Instrument, Inc.. It received FDA 510(k) clearance on 1990-11-05 under 510(k) number K900720. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED)?

MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED) is a medical device that received FDA 510(k) clearance on 1990-11-05. The listed applicant is Mortara Instrument, Inc.. The 510(k) number is K900720.

When did MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED) receive FDA 510(k) clearance?

MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED) received FDA 510(k) clearance on 1990-11-05, under 510(k) number K900720.

Who is the listed applicant for MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED)?

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

What is the FDA product code for MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED)?

The FDA product code for MORTARA INSTRUMENT MODEL X-SCRIBE (TREADMILL INCLUDED) is DSI.

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 Mortara Instrument, 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 47 devices →

Related Devices (Code: DSI)

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

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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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