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FDA 510(k)

L/U ARM-VASCULAR

K-Number: K781571 · 1978-11-27

ApplicantGeneral Electric Co.
Decision Date1978-11-27
Product CodeIYB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

L/U ARM-VASCULAR is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1978-11-27 under 510(k) number K781571. 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 L/U ARM-VASCULAR?

L/U ARM-VASCULAR is a medical device that received FDA 510(k) clearance on 1978-11-27. The listed applicant is General Electric Co.. The 510(k) number is K781571.

When did L/U ARM-VASCULAR receive FDA 510(k) clearance?

L/U ARM-VASCULAR received FDA 510(k) clearance on 1978-11-27, under 510(k) number K781571.

Who is the listed applicant for L/U ARM-VASCULAR?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for L/U ARM-VASCULAR?

The FDA product code for L/U ARM-VASCULAR is IYB.

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Other records listing General Electric Co. as applicant

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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.K941017F/C/W TUBESTANDAcoma Medical Imaging, Inc.K941004CTS SYSTEMAcoma 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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