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FDA 510(k)

BC/WT/PF

K-Number: K930249 · 1993-04-27

Decision Date1993-04-27
Product CodeIXY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BC/WT/PF is the device name listed in this FDA 510(k) record. The listed applicant is Tingle X-Ray Products, Inc.. It received FDA 510(k) clearance on 1993-04-27 under 510(k) number K930249. The device is classified under product code IXY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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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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