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FDA 510(k)

WAND PLUS

K-Number: K992819 · 2000-05-11

ApplicantSpintech, Inc.
Decision Date2000-05-11
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WAND PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Spintech, Inc.. It received FDA 510(k) clearance on 2000-05-11 under 510(k) number K992819. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WAND PLUS?

WAND PLUS is a medical device that received FDA 510(k) clearance on 2000-05-11. The listed applicant is Spintech, Inc.. The 510(k) number is K992819.

When did WAND PLUS receive FDA 510(k) clearance?

WAND PLUS received FDA 510(k) clearance on 2000-05-11, under 510(k) number K992819.

Who is the listed applicant for WAND PLUS?

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

What is the FDA product code for WAND PLUS?

The FDA product code for WAND PLUS is EJI.

Other records listing Spintech, 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.

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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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