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FDA 510(k)

NO POUR BASIN

K-Number: K840988 · 1984-03-07

ApplicantConcord Laboratories, Inc.
Decision Date1984-03-07
Product Code
DecisionUnknown

Device Summary

NO POUR BASIN 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 1984-03-07 under 510(k) number K840988. FDA Decision: Unknown.

Frequently Asked Questions

What is the NO POUR BASIN?

NO POUR BASIN is a medical device that received FDA 510(k) clearance on 1984-03-07. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K840988.

When did NO POUR BASIN receive FDA 510(k) clearance?

NO POUR BASIN received FDA 510(k) clearance on 1984-03-07, under 510(k) number K840988.

Who is the listed applicant for NO POUR BASIN?

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

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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. 6110K862039CONCORD CARE TRAYK854601SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATHK854327SUBCUTANEOUS TUNNELING NEEDLES & HANDLES

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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