CASTLE TEC-TEST STEAM STERI. INTEGRATOR
K-Number: K770078 · 1977-02-28
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Device Summary
Frequently Asked Questions
What is the CASTLE TEC-TEST STEAM STERI. INTEGRATOR?
CASTLE TEC-TEST STEAM STERI. INTEGRATOR is a medical device that received FDA 510(k) clearance on 1977-02-28. The listed applicant is Castle Co.. The 510(k) number is K770078.
When did CASTLE TEC-TEST STEAM STERI. INTEGRATOR receive FDA 510(k) clearance?
CASTLE TEC-TEST STEAM STERI. INTEGRATOR received FDA 510(k) clearance on 1977-02-28, under 510(k) number K770078.
Who is the listed applicant for CASTLE TEC-TEST STEAM STERI. INTEGRATOR?
The FDA 510(k) record lists Castle Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CASTLE TEC-TEST STEAM STERI. INTEGRATOR?
The FDA product code for CASTLE TEC-TEST STEAM STERI. INTEGRATOR is JOJ.
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 Castle Co. 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: JOJ)
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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