TEST SYSTEM TISSUE CELL CULTURE SLIDE
K-Number: K781516 · 1978-09-27
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Device Summary
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.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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