ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100
K-Number: K092245 · 2009-10-28
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Device Summary
Frequently Asked Questions
What is the ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100?
ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100 is a medical device that received FDA 510(k) clearance on 2009-10-28. The listed applicant is Honsun (Nantong) Co., Ltd.. The 510(k) number is K092245.
When did ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100 receive FDA 510(k) clearance?
ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100 received FDA 510(k) clearance on 2009-10-28, under 510(k) number K092245.
Who is the listed applicant for ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100?
The FDA 510(k) record lists Honsun (Nantong) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100?
The FDA product code for ANEROID SPHYGMOMANOMETER WITH STETHOSCOPE, MODEL LD-100 is DXQ.
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 Honsun (Nantong) Co., Ltd. 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: DXQ)
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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