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FDA 510(k)

SHARPOINT STAINLESS STEEL SUTURE

K-Number: K863034 · 1986-09-30

ApplicantChathamborough Research Group, Inc.
Decision Date1986-09-30
Product CodeGAO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHARPOINT STAINLESS STEEL SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Chathamborough Research Group, Inc.. It received FDA 510(k) clearance on 1986-09-30 under 510(k) number K863034. The device is classified under product code GAO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARPOINT STAINLESS STEEL SUTURE?

SHARPOINT STAINLESS STEEL SUTURE is a medical device that received FDA 510(k) clearance on 1986-09-30. The listed applicant is Chathamborough Research Group, Inc.. The 510(k) number is K863034.

When did SHARPOINT STAINLESS STEEL SUTURE receive FDA 510(k) clearance?

SHARPOINT STAINLESS STEEL SUTURE received FDA 510(k) clearance on 1986-09-30, under 510(k) number K863034.

Who is the listed applicant for SHARPOINT STAINLESS STEEL SUTURE?

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

What is the FDA product code for SHARPOINT STAINLESS STEEL SUTURE?

The FDA product code for SHARPOINT STAINLESS STEEL SUTURE is GAO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Chathamborough Research Group, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K915676SPLATTER SHIELDK904906SHARPOINT POLYPROPYLENE NONABSORB SURG SUTURES USPK902309PARKER MICROPUMP MODEL 2100

Related Devices (Code: GAO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K932513LABELING FOR MYO/WIRE II STERNOTOMY SUTURESAlto Development Corp.K872532AUTO SUTURE STAINLESS STEEL SUTURES*United States Surgical, A Division of Tyco HealthcK802248DISARP ORIGINALUnoplast A/S

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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