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FDA 510(k)

67-8006 DARLING-LINTON AORTIC TOURN.

K-Number: K761161 · 1976-12-06

ApplicantCodman & Shurtleff, Inc.
Decision Date1976-12-06
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

67-8006 DARLING-LINTON AORTIC TOURN. 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 1976-12-06 under 510(k) number K761161. 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 67-8006 DARLING-LINTON AORTIC TOURN.?

67-8006 DARLING-LINTON AORTIC TOURN. is a medical device that received FDA 510(k) clearance on 1976-12-06. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K761161.

When did 67-8006 DARLING-LINTON AORTIC TOURN. receive FDA 510(k) clearance?

67-8006 DARLING-LINTON AORTIC TOURN. received FDA 510(k) clearance on 1976-12-06, under 510(k) number K761161.

Who is the listed applicant for 67-8006 DARLING-LINTON AORTIC TOURN.?

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 67-8006 DARLING-LINTON AORTIC TOURN.?

The FDA product code for 67-8006 DARLING-LINTON AORTIC TOURN. 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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