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FDA 510(k)

FLUID MANAGEMENT SYSTEM

K-Number: K852645 · 1985-12-09

Decision Date1985-12-09
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLUID MANAGEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Haemonetics Corp.. It received FDA 510(k) clearance on 1985-12-09 under 510(k) number K852645. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUID MANAGEMENT SYSTEM?

FLUID MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1985-12-09. The listed applicant is Haemonetics Corp.. The 510(k) number is K852645.

When did FLUID MANAGEMENT SYSTEM receive FDA 510(k) clearance?

FLUID MANAGEMENT SYSTEM received FDA 510(k) clearance on 1985-12-09, under 510(k) number K852645.

Who is the listed applicant for FLUID MANAGEMENT SYSTEM?

The FDA 510(k) record lists Haemonetics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUID MANAGEMENT SYSTEM?

The FDA product code for FLUID MANAGEMENT SYSTEM is FRN.

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 Haemonetics Corp. 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 28 devices →

Related Devices (Code: FRN)

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.

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