THE KARL STORZ MODEL 28805 ARTHRO PUMP
K-Number: K871621 · 1987-06-05
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Device Summary
Frequently Asked Questions
What is the THE KARL STORZ MODEL 28805 ARTHRO PUMP?
THE KARL STORZ MODEL 28805 ARTHRO PUMP is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K871621.
When did THE KARL STORZ MODEL 28805 ARTHRO PUMP receive FDA 510(k) clearance?
THE KARL STORZ MODEL 28805 ARTHRO PUMP received FDA 510(k) clearance on 1987-06-05, under 510(k) number K871621.
Who is the listed applicant for THE KARL STORZ MODEL 28805 ARTHRO PUMP?
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 THE KARL STORZ MODEL 28805 ARTHRO PUMP?
The FDA product code for THE KARL STORZ MODEL 28805 ARTHRO PUMP 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.
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