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FDA 510(k)

SELVERSTONE CLAMP SALIBI CLAMP

K-Number: K870399 · 1987-03-06

ApplicantCodman & Shurtleff, Inc.
Decision Date1987-03-06
Product CodeHCE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SELVERSTONE CLAMP SALIBI CLAMP 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 1987-03-06 under 510(k) number K870399. The device is classified under product code HCE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELVERSTONE CLAMP SALIBI CLAMP?

SELVERSTONE CLAMP SALIBI CLAMP is a medical device that received FDA 510(k) clearance on 1987-03-06. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K870399.

When did SELVERSTONE CLAMP SALIBI CLAMP receive FDA 510(k) clearance?

SELVERSTONE CLAMP SALIBI CLAMP received FDA 510(k) clearance on 1987-03-06, under 510(k) number K870399.

Who is the listed applicant for SELVERSTONE CLAMP SALIBI CLAMP?

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 SELVERSTONE CLAMP SALIBI CLAMP?

The FDA product code for SELVERSTONE CLAMP SALIBI CLAMP is HCE.

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Related Devices (Code: HCE)

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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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