SIDE CUTTING PARALLEL ACTION PLIERS
K-Number: K872384 · 1987-07-02
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Device Summary
Frequently Asked Questions
What is the SIDE CUTTING PARALLEL ACTION PLIERS?
SIDE CUTTING PARALLEL ACTION PLIERS is a medical device that received FDA 510(k) clearance on 1987-07-02. The listed applicant is Med-Tool, Inc.. The 510(k) number is K872384.
When did SIDE CUTTING PARALLEL ACTION PLIERS receive FDA 510(k) clearance?
SIDE CUTTING PARALLEL ACTION PLIERS received FDA 510(k) clearance on 1987-07-02, under 510(k) number K872384.
Who is the listed applicant for SIDE CUTTING PARALLEL ACTION PLIERS?
The FDA 510(k) record lists Med-Tool, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIDE CUTTING PARALLEL ACTION PLIERS?
The FDA product code for SIDE CUTTING PARALLEL ACTION PLIERS is HTC.
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 Med-Tool, 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: HTC)
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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