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FDA 510(k)

HAEMONETICS LN 200F COLLECTION RESERVOIR

K-Number: K904474 · 1990-11-13

ApplicantHaemonetics Corp.
Decision Date1990-11-13
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HAEMONETICS LN 200F COLLECTION RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Haemonetics Corp.. It received FDA 510(k) clearance on 1990-11-13 under 510(k) number K904474. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAEMONETICS LN 200F COLLECTION RESERVOIR?

HAEMONETICS LN 200F COLLECTION RESERVOIR is a medical device that received FDA 510(k) clearance on 1990-11-13. The listed applicant is Haemonetics Corp.. The 510(k) number is K904474.

When did HAEMONETICS LN 200F COLLECTION RESERVOIR receive FDA 510(k) clearance?

HAEMONETICS LN 200F COLLECTION RESERVOIR received FDA 510(k) clearance on 1990-11-13, under 510(k) number K904474.

Who is the listed applicant for HAEMONETICS LN 200F COLLECTION RESERVOIR?

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 HAEMONETICS LN 200F COLLECTION RESERVOIR?

The FDA product code for HAEMONETICS LN 200F COLLECTION RESERVOIR is CAC.

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Other records listing Haemonetics Corp. as applicant

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Related Devices (Code: CAC)

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.

K241236XTRA Collection sets; XTRA Sequestration set XSorin Group Italia S.R.L.K240426Aventus Clot Management SystemInquis MedicalK240584XTRA Autotransfusion System (with XTRA Bowl sets)Sorin Group Italia S.R.L.K231782FlowSaver Blood Return System (80-101)Inari Medical, Inc.K221483FlowSaver Blood Return SystemInari Medical, Inc.K221722Haemonetics Cell Saver Elite/Elite+ Autotransfusion System (CSE-E-US/CSE-EW-US)Haemonetics Corporation

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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