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FDA 510(k)

MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS

K-Number: K041150 · 2004-07-22

Decision Date2004-07-22
Product CodeLRG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 2004-07-22 under 510(k) number K041150. The device is classified under product code LRG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS?

MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS is a medical device that received FDA 510(k) clearance on 2004-07-22. The listed applicant is Dade Behring, Inc.. The 510(k) number is K041150.

When did MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS receive FDA 510(k) clearance?

MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS received FDA 510(k) clearance on 2004-07-22, under 510(k) number K041150.

Who is the listed applicant for MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS?

The FDA 510(k) record lists Dade Behring, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS?

The FDA product code for MICROSCAN SYNERGIES PLUS GRAM-NEGATIVE MIC/COMBO PANELS is LRG.

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 Dade Behring, 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.

View all 343 devices →

Related Devices (Code: LRG)

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

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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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