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FDA 510(k)

VALTRAC (BAR) REMOVER DEVICE

K-Number: K863752 · 1986-10-24

ApplicantDavis & Geck, Inc.
Decision Date1986-10-24
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VALTRAC (BAR) REMOVER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1986-10-24 under 510(k) number K863752. The device is classified under product code EMF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALTRAC (BAR) REMOVER DEVICE?

VALTRAC (BAR) REMOVER DEVICE is a medical device that received FDA 510(k) clearance on 1986-10-24. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K863752.

When did VALTRAC (BAR) REMOVER DEVICE receive FDA 510(k) clearance?

VALTRAC (BAR) REMOVER DEVICE received FDA 510(k) clearance on 1986-10-24, under 510(k) number K863752.

Who is the listed applicant for VALTRAC (BAR) REMOVER DEVICE?

The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALTRAC (BAR) REMOVER DEVICE?

The FDA product code for VALTRAC (BAR) REMOVER DEVICE is EMF.

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Other records listing Davis & Geck, Inc. 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.

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Related Devices (Code: EMF)

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.

K080133MOUNTABLE ENDOSCOPIC BLADEA.M. Surgical, Inc.K982142MOUNTABLE ENDOSCOPIC KNIFEA.M. Surgical, Inc.K890217MICROSURGICAL KNIVESKinetic Medical ProductsK890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890214MICROSURGERY RAZOR BLADE HOLDERKinetic Medical ProductsK880094VAN-TEC ENDOPYELOTOMY KNIFEVan-Tec, 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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