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FDA 510(k)

RECOMED BLOOD-FLOW METER H236-052-02

K-Number: K840522 · 1985-05-16

ApplicantLitton Medical Electronics
Decision Date1985-05-16
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECOMED BLOOD-FLOW METER H236-052-02 is the device name listed in this FDA 510(k) record. The listed applicant is Litton Medical Electronics. It received FDA 510(k) clearance on 1985-05-16 under 510(k) number K840522. 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 RECOMED BLOOD-FLOW METER H236-052-02?

RECOMED BLOOD-FLOW METER H236-052-02 is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Litton Medical Electronics. The 510(k) number is K840522.

When did RECOMED BLOOD-FLOW METER H236-052-02 receive FDA 510(k) clearance?

RECOMED BLOOD-FLOW METER H236-052-02 received FDA 510(k) clearance on 1985-05-16, under 510(k) number K840522.

Who is the listed applicant for RECOMED BLOOD-FLOW METER H236-052-02?

The FDA 510(k) record lists Litton Medical Electronics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RECOMED BLOOD-FLOW METER H236-052-02?

The FDA product code for RECOMED BLOOD-FLOW METER H236-052-02 is DPW.

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Other records listing Litton Medical Electronics 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.

K840439RECOMED CARDIAC OUTPUT METER 236067-K840899SERVOMED ARRHYCOMP CENTRAL MONITOR SYSK840523SERVOMED PULSE AMPLIFIER MODULE-206-K840524SERVOMED BASIC BEDSIDE UNIT SMV 110TPK840209SERVOMED MEDIVISION SCOPE SMV-235K840832SERVOMED OXCARDIORE SPIROGRAPH 324/111

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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

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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