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FDA 510(k)

MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00

K-Number: K863551 · 1986-10-03

ApplicantDepuy, Inc.
Decision Date1986-10-03
Product Code
DecisionSubstantially Equivalent

Device Summary

MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00 is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1986-10-03 under 510(k) number K863551. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00?

MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00 is a medical device that received FDA 510(k) clearance on 1986-10-03. The listed applicant is Depuy, Inc.. The 510(k) number is K863551.

When did MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00 receive FDA 510(k) clearance?

MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00 received FDA 510(k) clearance on 1986-10-03, under 510(k) number K863551.

Who is the listed applicant for MODIFIED MEDI-QUET TOURNIQUET, MODEL #2740-00?

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

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Other records listing Depuy, 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.

K043058PINNACLE CONSTRAINED ACETABULAR LINERSK042664LPS UPPER EXTREMITYK041085LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARYK033959LPSK040544DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062K021478DELTA SHOULDER

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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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