KSEA BIPOLAR GOAGULATING FORCEPS
K-Number: K962396 · 1996-08-27
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Device Summary
Frequently Asked Questions
What is the KSEA BIPOLAR GOAGULATING FORCEPS?
KSEA BIPOLAR GOAGULATING FORCEPS is a medical device that received FDA 510(k) clearance on 1996-08-27. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K962396.
When did KSEA BIPOLAR GOAGULATING FORCEPS receive FDA 510(k) clearance?
KSEA BIPOLAR GOAGULATING FORCEPS received FDA 510(k) clearance on 1996-08-27, under 510(k) number K962396.
Who is the listed applicant for KSEA BIPOLAR GOAGULATING 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 BIPOLAR GOAGULATING FORCEPS?
The FDA product code for KSEA BIPOLAR GOAGULATING FORCEPS is EOB.
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: EOB)
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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