ENDOCERVICAL ELECTRODE # 2
K-Number: K070877 · 2007-07-27
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Device Summary
Frequently Asked Questions
What is the ENDOCERVICAL ELECTRODE # 2?
ENDOCERVICAL ELECTRODE # 2 is a medical device that received FDA 510(k) clearance on 2007-07-27. The listed applicant is Modern Medical Equipment Mfg., Ltd.. The 510(k) number is K070877.
When did ENDOCERVICAL ELECTRODE # 2 receive FDA 510(k) clearance?
ENDOCERVICAL ELECTRODE # 2 received FDA 510(k) clearance on 2007-07-27, under 510(k) number K070877.
Who is the listed applicant for ENDOCERVICAL ELECTRODE # 2?
The FDA 510(k) record lists Modern Medical Equipment Mfg., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOCERVICAL ELECTRODE # 2?
The FDA product code for ENDOCERVICAL ELECTRODE # 2 is HGI.
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 Modern Medical Equipment Mfg., 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: HGI)
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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