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FDA 510(k)

GW 35 GUIDE WIRE

K-Number: K772147 · 1977-11-28

ApplicantSorensen Research
Decision Date1977-11-28
Product CodeFIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GW 35 GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1977-11-28 under 510(k) number K772147. The device is classified under product code FIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GW 35 GUIDE WIRE?

GW 35 GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is Sorensen Research. The 510(k) number is K772147.

When did GW 35 GUIDE WIRE receive FDA 510(k) clearance?

GW 35 GUIDE WIRE received FDA 510(k) clearance on 1977-11-28, under 510(k) number K772147.

Who is the listed applicant for GW 35 GUIDE WIRE?

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

What is the FDA product code for GW 35 GUIDE WIRE?

The FDA product code for GW 35 GUIDE WIRE is FIF.

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Other records listing Sorensen Research as applicant

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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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