CHROMA, MODEL: RZ153C
K-Number: K083382 · 2009-08-13
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Device Summary
Frequently Asked Questions
What is the CHROMA, MODEL: RZ153C?
CHROMA, MODEL: RZ153C is a medical device that received FDA 510(k) clearance on 2009-08-13. The listed applicant is Scottcare Corporation. The 510(k) number is K083382.
When did CHROMA, MODEL: RZ153C receive FDA 510(k) clearance?
CHROMA, MODEL: RZ153C received FDA 510(k) clearance on 2009-08-13, under 510(k) number K083382.
Who is the listed applicant for CHROMA, MODEL: RZ153C?
The FDA 510(k) record lists Scottcare Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHROMA, MODEL: RZ153C?
The FDA product code for CHROMA, MODEL: RZ153C is MWJ.
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 Scottcare Corporation 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: MWJ)
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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