SAIF-BOW
K-Number: K771706 · 1977-09-20
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Device Summary
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
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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