Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CMS 2000 SERIES TPN KITS

K-Number: K831964 · 1983-08-11

Decision Date1983-08-11
Product CodeFMC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CMS 2000 SERIES TPN KITS is the device name listed in this FDA 510(k) record. The listed applicant is Currie Medical Specialties, Inc.. It received FDA 510(k) clearance on 1983-08-11 under 510(k) number K831964. The device is classified under product code FMC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CMS 2000 SERIES TPN KITS?

CMS 2000 SERIES TPN KITS is a medical device that received FDA 510(k) clearance on 1983-08-11. The listed applicant is Currie Medical Specialties, Inc.. The 510(k) number is K831964.

When did CMS 2000 SERIES TPN KITS receive FDA 510(k) clearance?

CMS 2000 SERIES TPN KITS received FDA 510(k) clearance on 1983-08-11, under 510(k) number K831964.

Who is the listed applicant for CMS 2000 SERIES TPN KITS?

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

What is the FDA product code for CMS 2000 SERIES TPN KITS?

The FDA product code for CMS 2000 SERIES TPN KITS is FMC.

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.

Other records listing Currie Medical Specialties, 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.

View all 10 devices →

Related Devices (Code: FMC)

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.

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.

↑