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FDA 510(k)

L-LINEX-RAY FLUORESCENCE

K-Number: K911749 · 1991-08-20

ApplicantMontifore Medical Center
Decision Date1991-08-20
Product CodeJAO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

L-LINEX-RAY FLUORESCENCE is the device name listed in this FDA 510(k) record. The listed applicant is Montifore Medical Center. It received FDA 510(k) clearance on 1991-08-20 under 510(k) number K911749. The device is classified under product code JAO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the L-LINEX-RAY FLUORESCENCE?

L-LINEX-RAY FLUORESCENCE is a medical device that received FDA 510(k) clearance on 1991-08-20. The listed applicant is Montifore Medical Center. The 510(k) number is K911749.

When did L-LINEX-RAY FLUORESCENCE receive FDA 510(k) clearance?

L-LINEX-RAY FLUORESCENCE received FDA 510(k) clearance on 1991-08-20, under 510(k) number K911749.

Who is the listed applicant for L-LINEX-RAY FLUORESCENCE?

The FDA 510(k) record lists Montifore Medical Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L-LINEX-RAY FLUORESCENCE?

The FDA product code for L-LINEX-RAY FLUORESCENCE is JAO.

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Related Devices (Code: JAO)

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.

K900574ABIOMED BODY LEAD ANALYZER MODEL 200/20Abiomed, Inc.

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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