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FDA 510(k)

MODEL C2-5000 OVERHEAD TUBE SUPPORT

K-Number: K873283 · 1987-09-10

ApplicantTransworld X-Ray Corp.
Decision Date1987-09-10
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL C2-5000 OVERHEAD TUBE SUPPORT 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 1987-09-10 under 510(k) number K873283. The device is classified under product code IYB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL C2-5000 OVERHEAD TUBE SUPPORT?

MODEL C2-5000 OVERHEAD TUBE SUPPORT is a medical device that received FDA 510(k) clearance on 1987-09-10. The listed applicant is Transworld X-Ray Corp.. The 510(k) number is K873283.

When did MODEL C2-5000 OVERHEAD TUBE SUPPORT receive FDA 510(k) clearance?

MODEL C2-5000 OVERHEAD TUBE SUPPORT received FDA 510(k) clearance on 1987-09-10, under 510(k) number K873283.

Who is the listed applicant for MODEL C2-5000 OVERHEAD TUBE SUPPORT?

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 MODEL C2-5000 OVERHEAD TUBE SUPPORT?

The FDA product code for MODEL C2-5000 OVERHEAD TUBE SUPPORT is IYB.

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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 36K872980MAM-CP X-RAY APPARATUSK872357TRANSWORLD 360V, MODEL A1-4040K841923DCX-100 CHEST UNIT-GL-5000MK827582MODIFIED X-RAY TABLE

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Related Devices (Code: IYB)

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.

K935123SUPERSTAND 300Wuestec Medical, Inc.K946261MTS-007, STS-008, SSMTS-010, EURO-40, 72, SUPER EURO 4072, 5000Scott Imaging Intl., Inc.K941004CTS SYSTEMAcoma Medical Imaging, Inc.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K940442MPR-814Xri, Inc.K935004MODEL ALPHA TS-2Dpa Consulting, 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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