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FDA 510(k)

HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS.

K-Number: K872895 · 1988-01-11

ApplicantHaemonetics Corp.
Decision Date1988-01-11
Product CodeCAL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS. is the device name listed in this FDA 510(k) record. The listed applicant is Haemonetics Corp.. It received FDA 510(k) clearance on 1988-01-11 under 510(k) number K872895. The device is classified under product code CAL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS.?

HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS. is a medical device that received FDA 510(k) clearance on 1988-01-11. The listed applicant is Haemonetics Corp.. The 510(k) number is K872895.

When did HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS. receive FDA 510(k) clearance?

HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS. received FDA 510(k) clearance on 1988-01-11, under 510(k) number K872895.

Who is the listed applicant for HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS.?

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 CELL SAVER MINI SAVER AUTO. BLOOD SYS.?

The FDA product code for HAEMONETICS CELL SAVER MINI SAVER AUTO. BLOOD SYS. is CAL.

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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.

K122262ORTHOPAT ADVANCE PERIOPERATIVE AUTOTRANSFUSION SYSTEMK120586CELL SAVER ELITEK101907HAEMONETICS CELL SAVER ELITE AUTOTRANSFUSION SYSTEMK062801SMARTSUCTION SOLO DEVICEK061103HAEMONETICS 40U RBC FILTER BAGK053000HAEMONETICS CARDIOVASCULAR PERIOPERATIVE AUTOTRANSFUSION SYSTEM (CARDIOPAT)

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Related Devices (Code: CAL)

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.

K951195FI-10PPentax Precision Instrument Corp.K951194FI-10MPentax Precision Instrument Corp.K852994REICHERT FLEXIBLE LARYNGOSCOPE, MODEL LS-11Reichert-Jung, Inc.K850978OLYMPUS LF-1 INTUBATION SCOPEOlympus Corp.K802331AO FLEXIBLE LARYNGOSCOPE, #LS-7American Optical Corp.K801364AO STYLET LARYNGOSCOPE MODEL SLSAmerican Optical Corp.

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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