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FDA 510(k)

PEDI-SPIDER STRAP

K-Number: K061721 · 2006-08-17

ApplicantEmergency Products and Research
Decision Date2006-08-17
Product CodeNZD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PEDI-SPIDER STRAP is the device name listed in this FDA 510(k) record. The listed applicant is Emergency Products and Research. It received FDA 510(k) clearance on 2006-08-17 under 510(k) number K061721. The device is classified under product code NZD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDI-SPIDER STRAP?

PEDI-SPIDER STRAP is a medical device that received FDA 510(k) clearance on 2006-08-17. The listed applicant is Emergency Products and Research. The 510(k) number is K061721.

When did PEDI-SPIDER STRAP receive FDA 510(k) clearance?

PEDI-SPIDER STRAP received FDA 510(k) clearance on 2006-08-17, under 510(k) number K061721.

Who is the listed applicant for PEDI-SPIDER STRAP?

The FDA 510(k) record lists Emergency Products and Research as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEDI-SPIDER STRAP?

The FDA product code for PEDI-SPIDER STRAP is NZD.

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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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