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FDA 510(k)

SAIF-BOW

K-Number: K771706 · 1977-09-20

Decision Date1977-09-20
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SAIF-BOW 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 1977-09-20 under 510(k) number K771706. 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 SAIF-BOW?

SAIF-BOW is a medical device that received FDA 510(k) clearance on 1977-09-20. The listed applicant is Northwest Orthodontics, Inc.. The 510(k) number is K771706.

When did SAIF-BOW receive FDA 510(k) clearance?

SAIF-BOW received FDA 510(k) clearance on 1977-09-20, under 510(k) number K771706.

Who is the listed applicant for SAIF-BOW?

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 SAIF-BOW?

The FDA product code for SAIF-BOW 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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