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FDA 510(k)

DISPOS. SCOTT CANNULAS 16-1054 ETC.

K-Number: K834477 · 1984-03-19

ApplicantCodman & Shurtleff, Inc.
Decision Date1984-03-19
Product CodeHCA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DISPOS. SCOTT CANNULAS 16-1054 ETC. 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 1984-03-19 under 510(k) number K834477. The device is classified under product code HCA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOS. SCOTT CANNULAS 16-1054 ETC.?

DISPOS. SCOTT CANNULAS 16-1054 ETC. is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K834477.

When did DISPOS. SCOTT CANNULAS 16-1054 ETC. receive FDA 510(k) clearance?

DISPOS. SCOTT CANNULAS 16-1054 ETC. received FDA 510(k) clearance on 1984-03-19, under 510(k) number K834477.

Who is the listed applicant for DISPOS. SCOTT CANNULAS 16-1054 ETC.?

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 DISPOS. SCOTT CANNULAS 16-1054 ETC.?

The FDA product code for DISPOS. SCOTT CANNULAS 16-1054 ETC. is HCA.

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Related Devices (Code: HCA)

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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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