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FDA 510(k)

MODIFIED LASERFLO BLOOD PERFUSION MONITOR

K-Number: K864259 · 1987-02-20

ApplicantTsi, Inc.
Decision Date1987-02-20
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED LASERFLO BLOOD PERFUSION MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Tsi, Inc.. It received FDA 510(k) clearance on 1987-02-20 under 510(k) number K864259. The device is classified under product code DPW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED LASERFLO BLOOD PERFUSION MONITOR?

MODIFIED LASERFLO BLOOD PERFUSION MONITOR is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Tsi, Inc.. The 510(k) number is K864259.

When did MODIFIED LASERFLO BLOOD PERFUSION MONITOR receive FDA 510(k) clearance?

MODIFIED LASERFLO BLOOD PERFUSION MONITOR received FDA 510(k) clearance on 1987-02-20, under 510(k) number K864259.

Who is the listed applicant for MODIFIED LASERFLO BLOOD PERFUSION MONITOR?

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

What is the FDA product code for MODIFIED LASERFLO BLOOD PERFUSION MONITOR?

The FDA product code for MODIFIED LASERFLO BLOOD PERFUSION MONITOR is DPW.

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 Tsi, Inc. 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.

K896515LASERFLO BLOOD PERFUSION MONITOR, MODEL BPM2K875179MODIFIED LASERFLO BLOOD PERFUSION MONITOR, BPM403AK851057LASERFLO BLOOD PERFUSION MONITOR 403

Related Devices (Code: DPW)

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.

K260700BlueDop Vascular ExpertBlueDop Medical, Ltd.K252810FloPatch FP120Flosonics MedicalK251904VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)Remington Medical, Inc.K251114FloPatch FP120Flosonics MedicalK243852Elfor-LElfi-Tech , Ltd.K241583VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)Remington Medical, Inc.

Official Source

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