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FDA 510(k)

KEY VASCULAR LOOPS

K-Number: K896676 · 1990-02-27

ApplicantKey Surgical, Inc.
Decision Date1990-02-27
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KEY VASCULAR LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Key Surgical, Inc.. It received FDA 510(k) clearance on 1990-02-27 under 510(k) number K896676. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEY VASCULAR LOOPS?

KEY VASCULAR LOOPS is a medical device that received FDA 510(k) clearance on 1990-02-27. The listed applicant is Key Surgical, Inc.. The 510(k) number is K896676.

When did KEY VASCULAR LOOPS receive FDA 510(k) clearance?

KEY VASCULAR LOOPS received FDA 510(k) clearance on 1990-02-27, under 510(k) number K896676.

Who is the listed applicant for KEY VASCULAR LOOPS?

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

What is the FDA product code for KEY VASCULAR LOOPS?

The FDA product code for KEY VASCULAR LOOPS is KDC.

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 Key Surgical, 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.

K910328KEY COMFORT GRIPSK896472KEY VASCULAR BOOTIESK895591SILICONE INSTRUMENT SHODS

Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, 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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