ARTHROSCOPY KNIVES
K-Number: K842820 · 1984-08-14
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Device Summary
Frequently Asked Questions
What is the ARTHROSCOPY KNIVES?
ARTHROSCOPY KNIVES is a medical device that received FDA 510(k) clearance on 1984-08-14. The listed applicant is Medtech Industries, Inc.. The 510(k) number is K842820.
When did ARTHROSCOPY KNIVES receive FDA 510(k) clearance?
ARTHROSCOPY KNIVES received FDA 510(k) clearance on 1984-08-14, under 510(k) number K842820.
Who is the listed applicant for ARTHROSCOPY KNIVES?
The FDA 510(k) record lists Medtech Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTHROSCOPY KNIVES?
The FDA product code for ARTHROSCOPY KNIVES is HTS.
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 Medtech Industries, 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: HTS)
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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