KS-78 VERTICAL WALL CASSETTE HOLDER
K-Number: K790742 · 1979-04-26
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Device Summary
Frequently Asked Questions
What is the KS-78 VERTICAL WALL CASSETTE HOLDER?
KS-78 VERTICAL WALL CASSETTE HOLDER is a medical device that received FDA 510(k) clearance on 1979-04-26. The listed applicant is Pausch Corp.. The 510(k) number is K790742.
When did KS-78 VERTICAL WALL CASSETTE HOLDER receive FDA 510(k) clearance?
KS-78 VERTICAL WALL CASSETTE HOLDER received FDA 510(k) clearance on 1979-04-26, under 510(k) number K790742.
Who is the listed applicant for KS-78 VERTICAL WALL CASSETTE HOLDER?
The FDA 510(k) record lists Pausch Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KS-78 VERTICAL WALL CASSETTE HOLDER?
The FDA product code for KS-78 VERTICAL WALL CASSETTE HOLDER is IXY.
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 Pausch Corp. 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.
Related Devices (Code: IXY)
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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