AT HOME DRUG CUP, MODEL 9150X
K-Number: K030447 · 2003-04-14
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Device Summary
Frequently Asked Questions
What is the AT HOME DRUG CUP, MODEL 9150X?
AT HOME DRUG CUP, MODEL 9150X is a medical device that received FDA 510(k) clearance on 2003-04-14. The listed applicant is Phamatech. The 510(k) number is K030447.
When did AT HOME DRUG CUP, MODEL 9150X receive FDA 510(k) clearance?
AT HOME DRUG CUP, MODEL 9150X received FDA 510(k) clearance on 2003-04-14, under 510(k) number K030447.
Who is the listed applicant for AT HOME DRUG CUP, MODEL 9150X?
The FDA 510(k) record lists Phamatech as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AT HOME DRUG CUP, MODEL 9150X?
The FDA product code for AT HOME DRUG CUP, MODEL 9150X is MVO.
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 Phamatech 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: MVO)
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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