BC/WT/PF
K-Number: K930249 · 1993-04-27
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Device Summary
Frequently Asked Questions
What is the BC/WT/PF?
BC/WT/PF is a medical device that received FDA 510(k) clearance on 1993-04-27. The listed applicant is Tingle X-Ray Products, Inc.. The 510(k) number is K930249.
When did BC/WT/PF receive FDA 510(k) clearance?
BC/WT/PF received FDA 510(k) clearance on 1993-04-27, under 510(k) number K930249.
Who is the listed applicant for BC/WT/PF?
The FDA 510(k) record lists Tingle X-Ray Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BC/WT/PF?
The FDA product code for BC/WT/PF is IXY.
Other records listing Tingle X-Ray Products, 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: IXY)
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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