KSEA MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS
K-Number: K010345 · 2001-08-03
Advertisement
Device Summary
Frequently Asked Questions
What is the KSEA MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS?
KSEA MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS is a medical device that received FDA 510(k) clearance on 2001-08-03. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K010345.
When did KSEA MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS receive FDA 510(k) clearance?
KSEA MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS received FDA 510(k) clearance on 2001-08-03, under 510(k) number K010345.
Who is the listed applicant for KSEA MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS?
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 MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS?
The FDA product code for KSEA MANHES TAKE-APART BIPOLAR COAGULATING FORCEPS is HRX.
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: HRX)
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