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FDA 510(k)

TRANSWORLD 360V, MODEL A1-4040

K-Number: K872357 · 1987-07-15

ApplicantTransworld X-Ray Corp.
Decision Date1987-07-15
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TRANSWORLD 360V, MODEL A1-4040 is the device name listed in this FDA 510(k) record. The listed applicant is Transworld X-Ray Corp.. It received FDA 510(k) clearance on 1987-07-15 under 510(k) number K872357. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSWORLD 360V, MODEL A1-4040?

TRANSWORLD 360V, MODEL A1-4040 is a medical device that received FDA 510(k) clearance on 1987-07-15. The listed applicant is Transworld X-Ray Corp.. The 510(k) number is K872357.

When did TRANSWORLD 360V, MODEL A1-4040 receive FDA 510(k) clearance?

TRANSWORLD 360V, MODEL A1-4040 received FDA 510(k) clearance on 1987-07-15, under 510(k) number K872357.

Who is the listed applicant for TRANSWORLD 360V, MODEL A1-4040?

The FDA 510(k) record lists Transworld X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSWORLD 360V, MODEL A1-4040?

The FDA product code for TRANSWORLD 360V, MODEL A1-4040 is IZO.

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Other records listing Transworld X-Ray Corp. 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.

K892657SENSIMATK890066STAR 36K873283MODEL C2-5000 OVERHEAD TUBE SUPPORTK872980MAM-CP X-RAY APPARATUSK841923DCX-100 CHEST UNIT-GL-5000MK827582MODIFIED X-RAY TABLE

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Related Devices (Code: IZO)

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.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, Inc.

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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