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FDA 510(k)

MORTARA INSTRUMENT MODEL ELI-XR (TREADMILL INCLUDED)

K-Number: K880664 · 1988-03-09

ApplicantMortara Instrument, Inc.
Decision Date1988-03-09
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MORTARA INSTRUMENT MODEL ELI-XR (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 1988-03-09 under 510(k) number K880664. 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 ELI-XR (TREADMILL INCLUDED)?

MORTARA INSTRUMENT MODEL ELI-XR (TREADMILL INCLUDED) is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is Mortara Instrument, Inc.. The 510(k) number is K880664.

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

MORTARA INSTRUMENT MODEL ELI-XR (TREADMILL INCLUDED) received FDA 510(k) clearance on 1988-03-09, under 510(k) number K880664.

Who is the listed applicant for MORTARA INSTRUMENT MODEL ELI-XR (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 ELI-XR (TREADMILL INCLUDED)?

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

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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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