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FDA 510(k)

DESILET

K-Number: K813143 · 1981-11-27

ApplicantExco, Inc.
Decision Date1981-11-27
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DESILET is the device name listed in this FDA 510(k) record. The listed applicant is Exco, Inc.. It received FDA 510(k) clearance on 1981-11-27 under 510(k) number K813143. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DESILET?

DESILET is a medical device that received FDA 510(k) clearance on 1981-11-27. The listed applicant is Exco, Inc.. The 510(k) number is K813143.

When did DESILET receive FDA 510(k) clearance?

DESILET received FDA 510(k) clearance on 1981-11-27, under 510(k) number K813143.

Who is the listed applicant for DESILET?

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

What is the FDA product code for DESILET?

The FDA product code for DESILET is DYB.

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Other records listing Exco, Inc. as applicant

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Related Devices (Code: DYB)

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.

K253526NAMIC Dilator and SheathMedline Industries, LPK261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/ Microintroducer Kit / Microintroducer Kit (SIS05C); Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set / Microintroducer Kit / Microintroducer Kit (IS01); Introducer Kit / Microintroducer Kit / Introducer Set /Microintroducer Set / Micro Introducer Sheath Set / Introducer Sheath Set (NIS04)Hartman Medical Group, LLCK261242SimplGuidePendracareK261950Health Line Tearaway IntroducerHealth Line International CorporationK261492FieldFlex Steerable SheathCenterPoint Systems, LLCK260606Echo Large Bore Introducer SheathEcho Medical, LLC

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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