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FDA 510(k)

THE EXTRACTOR(TM)

K-Number: K873932 · 1987-11-20

ApplicantMolecular Biosystems, Inc.
Decision Date1987-11-20
Product CodeDKO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

THE EXTRACTOR(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Molecular Biosystems, Inc.. It received FDA 510(k) clearance on 1987-11-20 under 510(k) number K873932. The device is classified under product code DKO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE EXTRACTOR(TM)?

THE EXTRACTOR(TM) is a medical device that received FDA 510(k) clearance on 1987-11-20. The listed applicant is Molecular Biosystems, Inc.. The 510(k) number is K873932.

When did THE EXTRACTOR(TM) receive FDA 510(k) clearance?

THE EXTRACTOR(TM) received FDA 510(k) clearance on 1987-11-20, under 510(k) number K873932.

Who is the listed applicant for THE EXTRACTOR(TM)?

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

What is the FDA product code for THE EXTRACTOR(TM)?

The FDA product code for THE EXTRACTOR(TM) is DKO.

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Other records listing Molecular Biosystems, 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.

K874544SNAP(R) CAMPYLOBACTER CULTURE IDENT DIAGNOSTIC KITK873670SNAP CAMPYLOBACTOR DIAGNOSTIC KITK873565SNAP(R) ROTAVIRUS DIAGNOSTIC KIT

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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