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FDA 510(k)

HEMOVAC AUTOTRANSFUSION SYSTEM

K-Number: K920273 · 1993-01-28

ApplicantZimmer Patient Care Division
Decision Date1993-01-28
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HEMOVAC AUTOTRANSFUSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Patient Care Division. It received FDA 510(k) clearance on 1993-01-28 under 510(k) number K920273. 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 HEMOVAC AUTOTRANSFUSION SYSTEM?

HEMOVAC AUTOTRANSFUSION SYSTEM is a medical device that received FDA 510(k) clearance on 1993-01-28. The listed applicant is Zimmer Patient Care Division. The 510(k) number is K920273.

When did HEMOVAC AUTOTRANSFUSION SYSTEM receive FDA 510(k) clearance?

HEMOVAC AUTOTRANSFUSION SYSTEM received FDA 510(k) clearance on 1993-01-28, under 510(k) number K920273.

Who is the listed applicant for HEMOVAC AUTOTRANSFUSION SYSTEM?

The FDA 510(k) record lists Zimmer Patient Care Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMOVAC AUTOTRANSFUSION SYSTEM?

The FDA product code for HEMOVAC AUTOTRANSFUSION SYSTEM is CAC.

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.

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Other records listing Zimmer Patient Care Division 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.

K963435ECONOMY SAFETY VEST RESTRAINT, SHOULDER TIE SAFETY VEST/SAFETY VEST RESTRAINT, HEAVY DUTY VEST RESTRAINT, MESH SAFETY VEK935709GENERAL SURGERY PROBE/GENERAL SURGERY PROBE W/DISTAL PERFORATIONS

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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