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FDA 510(k)

HUANG VEIN HOLDER, #21-8011

K-Number: K771026 · 1977-06-20

ApplicantCodman & Shurtleff, Inc.
Decision Date1977-06-20
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HUANG VEIN HOLDER, #21-8011 is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1977-06-20 under 510(k) number K771026. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUANG VEIN HOLDER, #21-8011?

HUANG VEIN HOLDER, #21-8011 is a medical device that received FDA 510(k) clearance on 1977-06-20. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K771026.

When did HUANG VEIN HOLDER, #21-8011 receive FDA 510(k) clearance?

HUANG VEIN HOLDER, #21-8011 received FDA 510(k) clearance on 1977-06-20, under 510(k) number K771026.

Who is the listed applicant for HUANG VEIN HOLDER, #21-8011?

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

What is the FDA product code for HUANG VEIN HOLDER, #21-8011?

The FDA product code for HUANG VEIN HOLDER, #21-8011 is DWS.

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Related Devices (Code: DWS)

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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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