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FDA 510(k)

TEST SYSTEM TISSUE CELL CULTURE SLIDE

K-Number: K781516 · 1978-09-27

Decision Date1978-09-27
Product CodeKIY
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TEST SYSTEM TISSUE CELL CULTURE SLIDE is the device name listed in this FDA 510(k) record. The listed applicant is Zeus Scientific, Inc.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781516. The device is classified under product code KIY. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEST SYSTEM TISSUE CELL CULTURE SLIDE?

TEST SYSTEM TISSUE CELL CULTURE SLIDE is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Zeus Scientific, Inc.. The 510(k) number is K781516.

When did TEST SYSTEM TISSUE CELL CULTURE SLIDE receive FDA 510(k) clearance?

TEST SYSTEM TISSUE CELL CULTURE SLIDE received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781516.

Who is the listed applicant for TEST SYSTEM TISSUE CELL CULTURE SLIDE?

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

What is the FDA product code for TEST SYSTEM TISSUE CELL CULTURE SLIDE?

The FDA product code for TEST SYSTEM TISSUE CELL CULTURE SLIDE is KIY.

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 Zeus Scientific, 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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