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FDA 510(k)

ADVANCE LASER FLOWMETER, ALF 21

K-Number: K903633 · 1990-10-09

ApplicantTransonic Systems, Inc.
Decision Date1990-10-09
Product CodeDPW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADVANCE LASER FLOWMETER, ALF 21 is the device name listed in this FDA 510(k) record. The listed applicant is Transonic Systems, Inc.. It received FDA 510(k) clearance on 1990-10-09 under 510(k) number K903633. 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 ADVANCE LASER FLOWMETER, ALF 21?

ADVANCE LASER FLOWMETER, ALF 21 is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Transonic Systems, Inc.. The 510(k) number is K903633.

When did ADVANCE LASER FLOWMETER, ALF 21 receive FDA 510(k) clearance?

ADVANCE LASER FLOWMETER, ALF 21 received FDA 510(k) clearance on 1990-10-09, under 510(k) number K903633.

Who is the listed applicant for ADVANCE LASER FLOWMETER, ALF 21?

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

What is the FDA product code for ADVANCE LASER FLOWMETER, ALF 21?

The FDA product code for ADVANCE LASER FLOWMETER, ALF 21 is DPW.

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Other records listing Transonic Systems, 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.

K113821TRANSONIC COSTATUS CARDIAC OUTPUT SYSTEMK112657AUREFLO MONITORING SYSTEMK080116TRANSONIC COSTATUS CARDIAC OUTPUT SYSTEMK033424ANGIOFLOW METER, ANGIOFLOW ANTEGRADE CATHETER, ANGIOFLOW RETROGRADE CATHETER, MODELS HVT100, ADT1001, ADT1002K022963TRANSONIC SYRINGE WARMER, MODEL SYR-1000K021571TRANSONIC FLOW-QC SET MODEL ADT1010

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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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