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FDA 510(k)

MORTARA INSTRUMENT MODEL ELI 50

K-Number: K902652 · 1990-08-23

ApplicantMortara Instrument, Inc.
Decision Date1990-08-23
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MORTARA INSTRUMENT MODEL ELI 50 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 1990-08-23 under 510(k) number K902652. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORTARA INSTRUMENT MODEL ELI 50?

MORTARA INSTRUMENT MODEL ELI 50 is a medical device that received FDA 510(k) clearance on 1990-08-23. The listed applicant is Mortara Instrument, Inc.. The 510(k) number is K902652.

When did MORTARA INSTRUMENT MODEL ELI 50 receive FDA 510(k) clearance?

MORTARA INSTRUMENT MODEL ELI 50 received FDA 510(k) clearance on 1990-08-23, under 510(k) number K902652.

Who is the listed applicant for MORTARA INSTRUMENT MODEL ELI 50?

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 50?

The FDA product code for MORTARA INSTRUMENT MODEL ELI 50 is DRT.

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Other records listing Mortara Instrument, Inc. as applicant

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Related Devices (Code: DRT)

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.

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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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