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FDA 510(k)

STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA.

K-Number: K881749 · 1988-07-18

ApplicantMedtronic Vascular
Decision Date1988-07-18
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA. is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K881749. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA.?

STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA. is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Medtronic Vascular. The 510(k) number is K881749.

When did STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA. receive FDA 510(k) clearance?

STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA. received FDA 510(k) clearance on 1988-07-18, under 510(k) number K881749.

Who is the listed applicant for STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA.?

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

What is the FDA product code for STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA.?

The FDA product code for STRAIGHT-LINE FINISH FOR IMPLANTABLE PULSE GENERA. is GXY.

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Related Devices (Code: GXY)

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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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