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FDA 510(k)

CONCORD CARE TRAY

K-Number: K862039 · 1986-07-03

ApplicantConcord Laboratories, Inc.
Decision Date1986-07-03
Product Code
DecisionUnknown

Device Summary

CONCORD CARE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Concord Laboratories, Inc.. It received FDA 510(k) clearance on 1986-07-03 under 510(k) number K862039. FDA Decision: Unknown.

Frequently Asked Questions

What is the CONCORD CARE TRAY?

CONCORD CARE TRAY is a medical device that received FDA 510(k) clearance on 1986-07-03. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K862039.

When did CONCORD CARE TRAY receive FDA 510(k) clearance?

CONCORD CARE TRAY received FDA 510(k) clearance on 1986-07-03, under 510(k) number K862039.

Who is the listed applicant for CONCORD CARE TRAY?

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

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 Concord Laboratories, 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.

K883840DRI-VENT ARTERIAL BLOOD SAMPLING KITK871825MECONIUM SUCTION CATHETERK864535TRACHEOBRONCHIAL SUCTION CATHETER, CAT. NO. 6110K854601SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATHK854327SUBCUTANEOUS TUNNELING NEEDLES & HANDLESK851134REGIONAL ANESTHESIA TRAYS

View all 42 devices →

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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