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FDA 510(k)

DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG

K-Number: K870201 · 1987-04-29

Decision Date1987-04-29
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1987-04-29 under 510(k) number K870201. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG?

DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG is a medical device that received FDA 510(k) clearance on 1987-04-29. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K870201.

When did DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG receive FDA 510(k) clearance?

DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG received FDA 510(k) clearance on 1987-04-29, under 510(k) number K870201.

Who is the listed applicant for DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG?

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

What is the FDA product code for DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG?

The FDA product code for DISPENS-O-DISC BROTH ELUTION DISKS METRON. 80 MCG is JTN.

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 Difco Laboratories, 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 121 devices →

Related Devices (Code: JTN)

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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