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FDA 510(k)

SNAP-WAY

K-Number: K790843 · 1979-05-31

Decision Date1979-05-31
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SNAP-WAY is the device name listed in this FDA 510(k) record. The listed applicant is Northwest Orthodontics, Inc.. It received FDA 510(k) clearance on 1979-05-31 under 510(k) number K790843. The device is classified under product code DZB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SNAP-WAY?

SNAP-WAY is a medical device that received FDA 510(k) clearance on 1979-05-31. The listed applicant is Northwest Orthodontics, Inc.. The 510(k) number is K790843.

When did SNAP-WAY receive FDA 510(k) clearance?

SNAP-WAY received FDA 510(k) clearance on 1979-05-31, under 510(k) number K790843.

Who is the listed applicant for SNAP-WAY?

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

What is the FDA product code for SNAP-WAY?

The FDA product code for SNAP-WAY is DZB.

Other records listing Northwest Orthodontics, 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.

Related Devices (Code: DZB)

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.

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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