NEO-VAGINA SURGERY SET AND ACCESSORIES
K-Number: K071754 · 2009-01-07
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Device Summary
Frequently Asked Questions
What is the NEO-VAGINA SURGERY SET AND ACCESSORIES?
NEO-VAGINA SURGERY SET AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2009-01-07. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K071754.
When did NEO-VAGINA SURGERY SET AND ACCESSORIES receive FDA 510(k) clearance?
NEO-VAGINA SURGERY SET AND ACCESSORIES received FDA 510(k) clearance on 2009-01-07, under 510(k) number K071754.
Who is the listed applicant for NEO-VAGINA SURGERY SET AND ACCESSORIES?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEO-VAGINA SURGERY SET AND ACCESSORIES?
The FDA product code for NEO-VAGINA SURGERY SET AND ACCESSORIES is HDX.
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 KARL STORZ Endoscopy-America, Inc. 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: HDX)
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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