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FDA 510(k)

MICROVASIVE INSURG LAPTIE SUTURE LIGATOR

K-Number: K931379 · 1993-07-13

ApplicantBoston Scientific Corp
Decision Date1993-07-13
Product CodeHCF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROVASIVE INSURG LAPTIE SUTURE LIGATOR is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K931379. The device is classified under product code HCF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROVASIVE INSURG LAPTIE SUTURE LIGATOR?

MICROVASIVE INSURG LAPTIE SUTURE LIGATOR is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Boston Scientific Corp. The 510(k) number is K931379.

When did MICROVASIVE INSURG LAPTIE SUTURE LIGATOR receive FDA 510(k) clearance?

MICROVASIVE INSURG LAPTIE SUTURE LIGATOR received FDA 510(k) clearance on 1993-07-13, under 510(k) number K931379.

Who is the listed applicant for MICROVASIVE INSURG LAPTIE SUTURE LIGATOR?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROVASIVE INSURG LAPTIE SUTURE LIGATOR?

The FDA product code for MICROVASIVE INSURG LAPTIE SUTURE LIGATOR is HCF.

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Other records listing Boston Scientific Corp as applicant

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Related Devices (Code: HCF)

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.

K851452VALTRAC PURSESTING DEVICEDavis & Geck, Inc.K841617STROVER HOOKPlastafil, Inc.K790577HEMORRHOIDAL LIGATORJ. Sklar Mfg. Co., Inc.

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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