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FDA 510(k)

MEDI-TEST COMBI 11

K-Number: K991927 · 1999-09-17

ApplicantMacherey-Nagel-Duren
Decision Date1999-09-17
Product CodeJIL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MEDI-TEST COMBI 11 is the device name listed in this FDA 510(k) record. The listed applicant is Macherey-Nagel-Duren. It received FDA 510(k) clearance on 1999-09-17 under 510(k) number K991927. The device is classified under product code JIL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-TEST COMBI 11?

MEDI-TEST COMBI 11 is a medical device that received FDA 510(k) clearance on 1999-09-17. The listed applicant is Macherey-Nagel-Duren. The 510(k) number is K991927.

When did MEDI-TEST COMBI 11 receive FDA 510(k) clearance?

MEDI-TEST COMBI 11 received FDA 510(k) clearance on 1999-09-17, under 510(k) number K991927.

Who is the listed applicant for MEDI-TEST COMBI 11?

The FDA 510(k) record lists Macherey-Nagel-Duren as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-TEST COMBI 11?

The FDA product code for MEDI-TEST COMBI 11 is JIL.

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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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