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FDA 510(k)

SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE)

K-Number: K014161 · 2002-01-15

ApplicantSt. Jude Medical, Inc.
Decision Date2002-01-15
Product CodeKRH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE) is the device name listed in this FDA 510(k) record. The listed applicant is St. Jude Medical, Inc.. It received FDA 510(k) clearance on 2002-01-15 under 510(k) number K014161. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE)?

SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE) is a medical device that received FDA 510(k) clearance on 2002-01-15. The listed applicant is St. Jude Medical, Inc.. The 510(k) number is K014161.

When did SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE) receive FDA 510(k) clearance?

SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE) received FDA 510(k) clearance on 2002-01-15, under 510(k) number K014161.

Who is the listed applicant for SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE)?

The FDA 510(k) record lists St. Jude Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE)?

The FDA product code for SJM TAILOR ANNULOPLASTY RING MODEL TARP- (SIZE) is KRH.

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Related Devices (Code: KRH)

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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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