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FDA 510(k)

SEPCOR UNIT COLLECTION MONITOR

K-Number: K820712 · 1982-05-07

ApplicantSeparation Science Corp.
Decision Date1982-05-07
Product CodeKSQ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SEPCOR UNIT COLLECTION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Separation Science Corp.. It received FDA 510(k) clearance on 1982-05-07 under 510(k) number K820712. The device is classified under product code KSQ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEPCOR UNIT COLLECTION MONITOR?

SEPCOR UNIT COLLECTION MONITOR is a medical device that received FDA 510(k) clearance on 1982-05-07. The listed applicant is Separation Science Corp.. The 510(k) number is K820712.

When did SEPCOR UNIT COLLECTION MONITOR receive FDA 510(k) clearance?

SEPCOR UNIT COLLECTION MONITOR received FDA 510(k) clearance on 1982-05-07, under 510(k) number K820712.

Who is the listed applicant for SEPCOR UNIT COLLECTION MONITOR?

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

What is the FDA product code for SEPCOR UNIT COLLECTION MONITOR?

The FDA product code for SEPCOR UNIT COLLECTION MONITOR is KSQ.

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 Separation Science 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.

K813327SEPCOR TEMPERATURE MONITOR

Related Devices (Code: KSQ)

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.

K842746HYCEL ROTOR-MIXER AND/OR MULTIR&D Systems, Inc.K812533PLATELET AGITATORHelmer Labs, Inc.K810617MOBILE MATIC AUTOMATIC DONOR SCALELifeline Instruments, Inc.K802608HEMATIC BLOOD MIXERHelmer Labs, Inc.K800104ROYCO MODEL 951 CELL MIXERRoyco InstrumentsK780189PLATELET ROTATORTravenol Laboratories, S.A.

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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