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FDA 510(k)

SPLINTER TWEEZERS

K-Number: K910570 · 1991-05-31

ApplicantSolan Scissors Sales
Decision Date1991-05-31
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPLINTER TWEEZERS is the device name listed in this FDA 510(k) record. The listed applicant is Solan Scissors Sales. It received FDA 510(k) clearance on 1991-05-31 under 510(k) number K910570. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPLINTER TWEEZERS?

SPLINTER TWEEZERS is a medical device that received FDA 510(k) clearance on 1991-05-31. The listed applicant is Solan Scissors Sales. The 510(k) number is K910570.

When did SPLINTER TWEEZERS receive FDA 510(k) clearance?

SPLINTER TWEEZERS received FDA 510(k) clearance on 1991-05-31, under 510(k) number K910570.

Who is the listed applicant for SPLINTER TWEEZERS?

The FDA 510(k) record lists Solan Scissors Sales as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPLINTER TWEEZERS?

The FDA product code for SPLINTER TWEEZERS is FSM.

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Related Devices (Code: FSM)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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