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FDA 510(k)

525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR

K-Number: K926554 · 1993-05-17

ApplicantTingle X-Ray Products, Inc.
Decision Date1993-05-17
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR 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 1993-05-17 under 510(k) number K926554. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR?

525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Tingle X-Ray Products, Inc.. The 510(k) number is K926554.

When did 525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR receive FDA 510(k) clearance?

525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR received FDA 510(k) clearance on 1993-05-17, under 510(k) number K926554.

Who is the listed applicant for 525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR?

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 525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR?

The FDA product code for 525 SFQ X-RAY CONTROL W/HIGH VOLTAGE GENERATOR is KPR.

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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.

K930249BC/WT/PFK860203TXR 325 X-RAY CONTROL WITH HIGH VOLTAGE GENERATOR

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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