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FDA 510(k)

SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR

K-Number: K880717 · 1988-03-03

ApplicantRemel Co.
Decision Date1988-03-03
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1988-03-03 under 510(k) number K880717. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR?

SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Remel Co.. The 510(k) number is K880717.

When did SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR receive FDA 510(k) clearance?

SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR received FDA 510(k) clearance on 1988-03-03, under 510(k) number K880717.

Who is the listed applicant for SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR?

The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR?

The FDA product code for SLIDE CULTURE PLATE-POTATO DEXTROSE AGAR is JSJ.

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 Remel Co. 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 137 devices →

Related Devices (Code: JSJ)

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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