CASTLE 7515 UTENSIL/GLASSWARE WASHER
K-Number: K844089 · 1985-01-14
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Device Summary
Frequently Asked Questions
What is the CASTLE 7515 UTENSIL/GLASSWARE WASHER?
CASTLE 7515 UTENSIL/GLASSWARE WASHER is a medical device that received FDA 510(k) clearance on 1985-01-14. The listed applicant is Castle Co.. The 510(k) number is K844089.
When did CASTLE 7515 UTENSIL/GLASSWARE WASHER receive FDA 510(k) clearance?
CASTLE 7515 UTENSIL/GLASSWARE WASHER received FDA 510(k) clearance on 1985-01-14, under 510(k) number K844089.
Who is the listed applicant for CASTLE 7515 UTENSIL/GLASSWARE WASHER?
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 7515 UTENSIL/GLASSWARE WASHER?
The FDA product code for CASTLE 7515 UTENSIL/GLASSWARE WASHER is LDS.
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: LDS)
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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