STEAM STERILIZER, 3000
K-Number: K770536 · 1977-04-29
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Device Summary
Frequently Asked Questions
What is the STEAM STERILIZER, 3000?
STEAM STERILIZER, 3000 is a medical device that received FDA 510(k) clearance on 1977-04-29. The listed applicant is Castle Co.. The 510(k) number is K770536.
When did STEAM STERILIZER, 3000 receive FDA 510(k) clearance?
STEAM STERILIZER, 3000 received FDA 510(k) clearance on 1977-04-29, under 510(k) number K770536.
Who is the listed applicant for STEAM STERILIZER, 3000?
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 STEAM STERILIZER, 3000?
The FDA product code for STEAM STERILIZER, 3000 is FLE.
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: FLE)
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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