JASUN, MODELS DT-01F AND DT-11F
K-Number: K030361 · 2003-02-21
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Device Summary
Frequently Asked Questions
What is the JASUN, MODELS DT-01F AND DT-11F?
JASUN, MODELS DT-01F AND DT-11F is a medical device that received FDA 510(k) clearance on 2003-02-21. The listed applicant is Hangzhou Hua'An Medical & Health Instruments Co.,. The 510(k) number is K030361.
When did JASUN, MODELS DT-01F AND DT-11F receive FDA 510(k) clearance?
JASUN, MODELS DT-01F AND DT-11F received FDA 510(k) clearance on 2003-02-21, under 510(k) number K030361.
Who is the listed applicant for JASUN, MODELS DT-01F AND DT-11F?
The FDA 510(k) record lists Hangzhou Hua'An Medical & Health Instruments Co., as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JASUN, MODELS DT-01F AND DT-11F?
The FDA product code for JASUN, MODELS DT-01F AND DT-11F is FLL.
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 Hangzhou Hua'An Medical & Health Instruments 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: FLL)
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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