WEINGART MODEL 1000 SUNLAMP PRODUCT
K-Number: K863518 · 1986-10-02
Advertisement
Device Summary
Frequently Asked Questions
What is the WEINGART MODEL 1000 SUNLAMP PRODUCT?
WEINGART MODEL 1000 SUNLAMP PRODUCT is a medical device that received FDA 510(k) clearance on 1986-10-02. The listed applicant is Weingart, Inc.. The 510(k) number is K863518.
When did WEINGART MODEL 1000 SUNLAMP PRODUCT receive FDA 510(k) clearance?
WEINGART MODEL 1000 SUNLAMP PRODUCT received FDA 510(k) clearance on 1986-10-02, under 510(k) number K863518.
Who is the listed applicant for WEINGART MODEL 1000 SUNLAMP PRODUCT?
The FDA 510(k) record lists Weingart, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WEINGART MODEL 1000 SUNLAMP PRODUCT?
The FDA product code for WEINGART MODEL 1000 SUNLAMP PRODUCT is FTC.
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 Weingart, 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: FTC)
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.
Advertisement