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FDA 510(k)

BROTH ELUTION DISKS CLINDAMYCIN 10MCG

K-Number: K870175 · 1987-04-29

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

Device Summary

BROTH ELUTION DISKS CLINDAMYCIN 10MCG 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 K870175. 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 BROTH ELUTION DISKS CLINDAMYCIN 10MCG?

BROTH ELUTION DISKS CLINDAMYCIN 10MCG 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 K870175.

When did BROTH ELUTION DISKS CLINDAMYCIN 10MCG receive FDA 510(k) clearance?

BROTH ELUTION DISKS CLINDAMYCIN 10MCG received FDA 510(k) clearance on 1987-04-29, under 510(k) number K870175.

Who is the listed applicant for BROTH ELUTION DISKS CLINDAMYCIN 10MCG?

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 BROTH ELUTION DISKS CLINDAMYCIN 10MCG?

The FDA product code for BROTH ELUTION DISKS CLINDAMYCIN 10MCG 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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