CASTLE PROCEDURE AND RITTER EXAM. TABLES
K-Number: K810900 · 1981-04-21
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Device Summary
Frequently Asked Questions
What is the CASTLE PROCEDURE AND RITTER EXAM. TABLES?
CASTLE PROCEDURE AND RITTER EXAM. TABLES is a medical device that received FDA 510(k) clearance on 1981-04-21. The listed applicant is Sybron Corp.. The 510(k) number is K810900.
When did CASTLE PROCEDURE AND RITTER EXAM. TABLES receive FDA 510(k) clearance?
CASTLE PROCEDURE AND RITTER EXAM. TABLES received FDA 510(k) clearance on 1981-04-21, under 510(k) number K810900.
Who is the listed applicant for CASTLE PROCEDURE AND RITTER EXAM. TABLES?
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 CASTLE PROCEDURE AND RITTER EXAM. TABLES?
The FDA product code for CASTLE PROCEDURE AND RITTER EXAM. TABLES is LGX.
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: LGX)
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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