FDA 510(k)

SURGEONS CHOICE PI VASCULAR STAPLING

K-Number: K843399 · 1984-11-05

Decision Date1984-11-05

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SURGEONS CHOICE PI VASCULAR STAPLING is the device name listed in this FDA 510(k) record. The listed applicant is Surgeons Choice, Inc.. It received FDA 510(k) clearance on 1984-11-05 under 510(k) number K843399. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGEONS CHOICE PI VASCULAR STAPLING?

SURGEONS CHOICE PI VASCULAR STAPLING is a medical device that received FDA 510(k) clearance on 1984-11-05. The listed applicant is Surgeons Choice, Inc.. The 510(k) number is K843399.

When did SURGEONS CHOICE PI VASCULAR STAPLING receive FDA 510(k) clearance?

SURGEONS CHOICE PI VASCULAR STAPLING received FDA 510(k) clearance on 1984-11-05, under 510(k) number K843399.

Who is the listed applicant for SURGEONS CHOICE PI VASCULAR STAPLING?

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

What is the FDA product code for SURGEONS CHOICE PI VASCULAR STAPLING?

The FDA product code for SURGEONS CHOICE PI VASCULAR STAPLING is GDW.

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Other records listing Surgeons Choice, Inc. as applicant

K851121PI-PHEUMO INTESTINAL INSTRUMENT SET K851122PI-PNEUMO INTESTINAL STAPLING CARTRIDGE K830768DISPOSABLE SKIN STAPLER K823776PI-PNEUMO-INTESTINAL INSTRUMENT SET K813170ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER

Related Devices (Code: GDW)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.