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FDA 510(k)

MIDWEST LIGHT WAND

K-Number: K820693 · 1982-04-09

ApplicantAmerican Midwest
Decision Date1982-04-09
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIDWEST LIGHT WAND is the device name listed in this FDA 510(k) record. The listed applicant is American Midwest. It received FDA 510(k) clearance on 1982-04-09 under 510(k) number K820693. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDWEST LIGHT WAND?

MIDWEST LIGHT WAND is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is American Midwest. The 510(k) number is K820693.

When did MIDWEST LIGHT WAND receive FDA 510(k) clearance?

MIDWEST LIGHT WAND received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820693.

Who is the listed applicant for MIDWEST LIGHT WAND?

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

What is the FDA product code for MIDWEST LIGHT WAND?

The FDA product code for MIDWEST LIGHT WAND is EBZ.

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Other records listing American Midwest as applicant

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Related Devices (Code: EBZ)

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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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