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FDA 510(k)

Q.P. PREAMPLIFIER SYS

K-Number: K841683 · 1984-06-07

ApplicantBio-Scan, Inc.
Decision Date1984-06-07
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Q.P. PREAMPLIFIER SYS is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Scan, Inc.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K841683. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Q.P. PREAMPLIFIER SYS?

Q.P. PREAMPLIFIER SYS is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Bio-Scan, Inc.. The 510(k) number is K841683.

When did Q.P. PREAMPLIFIER SYS receive FDA 510(k) clearance?

Q.P. PREAMPLIFIER SYS received FDA 510(k) clearance on 1984-06-07, under 510(k) number K841683.

Who is the listed applicant for Q.P. PREAMPLIFIER SYS?

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

What is the FDA product code for Q.P. PREAMPLIFIER SYS?

The FDA product code for Q.P. PREAMPLIFIER SYS is GWQ.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Bio-Scan, 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.

K003480BIOFINDK925735EEG ANALYZERK864928BIO-LOG 8+1 AMBULATORY PHYSIOLOGIC RECORDERK841685EEG ELECTRODESK841684BIO/SCAN BIOLOG CASSETTE RECORDER

Related Devices (Code: GWQ)

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.

K261604Enobio Dx (Enobio Dx 8);Enobio Dx (Enobio Dx 20);Enobio Dx (Enobio Dx 32)Neuroelectrics Barcelona S.L.U.K260455New Wave SystemZeto, Inc.K233403Flexset SystemZeto, Inc.K231366Neuronaute PlusBioserenity SasK221959Q21Neurofield, Inc.K231457SPARK ScanSpark Neuro, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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