MORTARA INSTRUMENT ODEL ELI 50I
K-Number: K915730 · 1992-11-10
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Device Summary
Frequently Asked Questions
What is the MORTARA INSTRUMENT ODEL ELI 50I?
MORTARA INSTRUMENT ODEL ELI 50I is a medical device that received FDA 510(k) clearance on 1992-11-10. The listed applicant is Mortara Instrument, Inc.. The 510(k) number is K915730.
When did MORTARA INSTRUMENT ODEL ELI 50I receive FDA 510(k) clearance?
MORTARA INSTRUMENT ODEL ELI 50I received FDA 510(k) clearance on 1992-11-10, under 510(k) number K915730.
Who is the listed applicant for MORTARA INSTRUMENT ODEL ELI 50I?
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 ODEL ELI 50I?
The FDA product code for MORTARA INSTRUMENT ODEL ELI 50I is LOS.
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.
Related Devices (Code: LOS)
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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