SCISSOR, RIGHT
K-Number: K873502 · 1987-11-02
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Device Summary
Frequently Asked Questions
What is the SCISSOR, RIGHT?
SCISSOR, RIGHT is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873502.
When did SCISSOR, RIGHT receive FDA 510(k) clearance?
SCISSOR, RIGHT received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873502.
Who is the listed applicant for SCISSOR, RIGHT?
The FDA 510(k) record lists Arthropedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCISSOR, RIGHT?
The FDA product code for SCISSOR, RIGHT is HRR.
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 Arthropedics, 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: HRR)
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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