MODIFICATION TO NANMA VACUUM PUMP
K-Number: K013113 · 2002-12-20
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO NANMA VACUUM PUMP?
MODIFICATION TO NANMA VACUUM PUMP is a medical device that received FDA 510(k) clearance on 2002-12-20. The listed applicant is Nanma Mfg Co., Ltd.. The 510(k) number is K013113.
When did MODIFICATION TO NANMA VACUUM PUMP receive FDA 510(k) clearance?
MODIFICATION TO NANMA VACUUM PUMP received FDA 510(k) clearance on 2002-12-20, under 510(k) number K013113.
Who is the listed applicant for MODIFICATION TO NANMA VACUUM PUMP?
The FDA 510(k) record lists Nanma Mfg Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO NANMA VACUUM PUMP?
The FDA product code for MODIFICATION TO NANMA VACUUM PUMP is LKY.
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 Nanma Mfg 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: LKY)
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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