KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR
K-Number: K010346 · 2001-05-02
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Device Summary
Frequently Asked Questions
What is the KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR?
KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR is a medical device that received FDA 510(k) clearance on 2001-05-02. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K010346.
When did KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR receive FDA 510(k) clearance?
KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR received FDA 510(k) clearance on 2001-05-02, under 510(k) number K010346.
Who is the listed applicant for KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR?
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 KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR?
The FDA product code for KSEA SAWAHLE ELECTROMECHANICAL MORCELLATOR is GCJ.
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: GCJ)
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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