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FDA 510(k)

NEW FUCHSIN SOLUTION

K-Number: K871545 · 1987-04-29

Decision Date1987-04-29
Product CodeIDF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

NEW FUCHSIN SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-04-29 under 510(k) number K871545. The device is classified under product code IDF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW FUCHSIN SOLUTION?

NEW FUCHSIN SOLUTION is a medical device that received FDA 510(k) clearance on 1987-04-29. The listed applicant is Sigma Diagnostics, Inc.. The 510(k) number is K871545.

When did NEW FUCHSIN SOLUTION receive FDA 510(k) clearance?

NEW FUCHSIN SOLUTION received FDA 510(k) clearance on 1987-04-29, under 510(k) number K871545.

Who is the listed applicant for NEW FUCHSIN SOLUTION?

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

What is the FDA product code for NEW FUCHSIN SOLUTION?

The FDA product code for NEW FUCHSIN SOLUTION is IDF.

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 Sigma Diagnostics, 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.

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Official Source

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