RITTER MODEL H COMPANION STOOL
K-Number: K800276 · 1980-03-17
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Device Summary
Frequently Asked Questions
What is the RITTER MODEL H COMPANION STOOL?
RITTER MODEL H COMPANION STOOL is a medical device that received FDA 510(k) clearance on 1980-03-17. The listed applicant is Sybron Corp.. The 510(k) number is K800276.
When did RITTER MODEL H COMPANION STOOL receive FDA 510(k) clearance?
RITTER MODEL H COMPANION STOOL received FDA 510(k) clearance on 1980-03-17, under 510(k) number K800276.
Who is the listed applicant for RITTER MODEL H COMPANION STOOL?
The FDA 510(k) record lists Sybron Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RITTER MODEL H COMPANION STOOL?
The FDA product code for RITTER MODEL H COMPANION STOOL is KLC.
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 Sybron 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: KLC)
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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