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FDA 510(k)

GUIDE WIRE

K-Number: K874164 · 1987-12-07

ApplicantEndovations
Decision Date1987-12-07
Product CodeEZB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GUIDE WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Endovations. It received FDA 510(k) clearance on 1987-12-07 under 510(k) number K874164. The device is classified under product code EZB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUIDE WIRE?

GUIDE WIRE is a medical device that received FDA 510(k) clearance on 1987-12-07. The listed applicant is Endovations. The 510(k) number is K874164.

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

GUIDE WIRE received FDA 510(k) clearance on 1987-12-07, under 510(k) number K874164.

Who is the listed applicant for GUIDE WIRE?

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

What is the FDA product code for GUIDE WIRE?

The FDA product code for GUIDE WIRE is EZB.

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Other records listing Endovations 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.

K955413ENDOVATIONS TRIPLE LUMEN BALLOON DILATATION CATHETERK942110INJECT-SNAREK934315ENDOVATIONS(R) .035 PRE-CUT PAPILLATOMEK9138412 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATHK9138705MM MICROSCISSORSK911155OVAL CUP BIOPSY FORCEP

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Related Devices (Code: EZB)

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.

K971498APPLIED MEDICAL LAPAROSCOPIC GUIDEWIREApplied Medical ResourcesK970994CORE AND COIL ASSEMBLY GUIDEWIRELake Region Mfg., 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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