JOSEPH SAW
K-Number: K772379 · 1978-02-02
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Device Summary
Frequently Asked Questions
What is the JOSEPH SAW?
JOSEPH SAW is a medical device that received FDA 510(k) clearance on 1978-02-02. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772379.
When did JOSEPH SAW receive FDA 510(k) clearance?
JOSEPH SAW received FDA 510(k) clearance on 1978-02-02, under 510(k) number K772379.
Who is the listed applicant for JOSEPH SAW?
The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JOSEPH SAW?
The FDA product code for JOSEPH SAW is KBC.
Related Clinical Trials
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.
Other records listing Edward Weck, 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: KBC)
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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