MERITS E700 PORCE LIFT
K-Number: K073513 · 2008-01-14
Advertisement
Device Summary
Frequently Asked Questions
What is the MERITS E700 PORCE LIFT?
MERITS E700 PORCE LIFT is a medical device that received FDA 510(k) clearance on 2008-01-14. The listed applicant is Merits Health Products Co., Ltd.. The 510(k) number is K073513.
When did MERITS E700 PORCE LIFT receive FDA 510(k) clearance?
MERITS E700 PORCE LIFT received FDA 510(k) clearance on 2008-01-14, under 510(k) number K073513.
Who is the listed applicant for MERITS E700 PORCE LIFT?
The FDA 510(k) record lists Merits Health Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MERITS E700 PORCE LIFT?
The FDA product code for MERITS E700 PORCE LIFT is ING.
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 Merits Health Products 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: ING)
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.
Advertisement