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FDA 510(k)

MID-STREAM URINE COLLECTION SETS

K-Number: K840709 · 1984-04-03

ApplicantConcord Laboratories, Inc.
Decision Date1984-04-03
Product Code
DecisionSubstantially Equivalent

Device Summary

MID-STREAM URINE COLLECTION SETS 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 1984-04-03 under 510(k) number K840709. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MID-STREAM URINE COLLECTION SETS?

MID-STREAM URINE COLLECTION SETS is a medical device that received FDA 510(k) clearance on 1984-04-03. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K840709.

When did MID-STREAM URINE COLLECTION SETS receive FDA 510(k) clearance?

MID-STREAM URINE COLLECTION SETS received FDA 510(k) clearance on 1984-04-03, under 510(k) number K840709.

Who is the listed applicant for MID-STREAM URINE COLLECTION SETS?

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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