ARTHROSCOPE
K-Number: K971083 · 1997-06-23
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Device Summary
Frequently Asked Questions
What is the ARTHROSCOPE?
ARTHROSCOPE is a medical device that received FDA 510(k) clearance on 1997-06-23. The listed applicant is Electro-Biology, Inc.. The 510(k) number is K971083.
When did ARTHROSCOPE receive FDA 510(k) clearance?
ARTHROSCOPE received FDA 510(k) clearance on 1997-06-23, under 510(k) number K971083.
Who is the listed applicant for ARTHROSCOPE?
The FDA 510(k) record lists Electro-Biology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTHROSCOPE?
The FDA product code for ARTHROSCOPE 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 Electro-Biology, 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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