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FDA 510(k)

EZ SPLINT & EZ SPLINT PM

K-Number: K022809 · 2003-10-17

ApplicantPower Products, Inc.-Splintek
Decision Date2003-10-17
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

EZ SPLINT & EZ SPLINT PM is the device name listed in this FDA 510(k) record. The listed applicant is Power Products, Inc.-Splintek. It received FDA 510(k) clearance on 2003-10-17 under 510(k) number K022809. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ SPLINT & EZ SPLINT PM?

EZ SPLINT & EZ SPLINT PM is a medical device that received FDA 510(k) clearance on 2003-10-17. The listed applicant is Power Products, Inc.-Splintek. The 510(k) number is K022809.

When did EZ SPLINT & EZ SPLINT PM receive FDA 510(k) clearance?

EZ SPLINT & EZ SPLINT PM received FDA 510(k) clearance on 2003-10-17, under 510(k) number K022809.

Who is the listed applicant for EZ SPLINT & EZ SPLINT PM?

The FDA 510(k) record lists Power Products, Inc.-Splintek as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ SPLINT & EZ SPLINT PM?

The FDA product code for EZ SPLINT & EZ SPLINT PM is MQC.

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Other records listing Power Products, Inc.-Splintek 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.

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Related Devices (Code: MQC)

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

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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