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FDA 510(k)

WECK MICROSURGICAL KNIFE

K-Number: K791286 · 1979-07-24

ApplicantVista Medical Products, Inc.
Decision Date1979-07-24
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WECK MICROSURGICAL KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Vista Medical Products, Inc.. It received FDA 510(k) clearance on 1979-07-24 under 510(k) number K791286. 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 WECK MICROSURGICAL KNIFE?

WECK MICROSURGICAL KNIFE is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is Vista Medical Products, Inc.. The 510(k) number is K791286.

When did WECK MICROSURGICAL KNIFE receive FDA 510(k) clearance?

WECK MICROSURGICAL KNIFE received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791286.

Who is the listed applicant for WECK MICROSURGICAL KNIFE?

The FDA 510(k) record lists Vista Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WECK MICROSURGICAL KNIFE?

The FDA product code for WECK MICROSURGICAL KNIFE is EMF.

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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.K890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890217MICROSURGICAL KNIVESKinetic 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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