Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PEAKLOG AND DISPLAY SOFTWARE

K-Number: K940836 · 1994-11-01

ApplicantTamarac Systems Corp.
Decision Date1994-11-01
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEAKLOG AND DISPLAY SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Tamarac Systems Corp.. It received FDA 510(k) clearance on 1994-11-01 under 510(k) number K940836. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEAKLOG AND DISPLAY SOFTWARE?

PEAKLOG AND DISPLAY SOFTWARE is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Tamarac Systems Corp.. The 510(k) number is K940836.

When did PEAKLOG AND DISPLAY SOFTWARE receive FDA 510(k) clearance?

PEAKLOG AND DISPLAY SOFTWARE received FDA 510(k) clearance on 1994-11-01, under 510(k) number K940836.

Who is the listed applicant for PEAKLOG AND DISPLAY SOFTWARE?

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

What is the FDA product code for PEAKLOG AND DISPLAY SOFTWARE?

The FDA product code for PEAKLOG AND DISPLAY SOFTWARE is BZH.

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 Tamarac Systems 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.

K894997PRESTO DIAGNOSTIC SPIROMETERK894680RS232 FLOW SENSOR AND SOFTWARE PACKAGE

Related Devices (Code: BZH)

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.

K253180Microlife Digital Peak Flow Meter, Model PF200B (PF200B)Microlife CorporationK252802Peak Flow Meter (PF-10(BR-PEF231))Shenzhen Bi-Rich Medical Devices Co., Ltd.K241338Peak Flow MeterChongqing Moffy Innovation Technology Co., Ltd.K232588Aluna 2Knox Medical DiagnosticsK230423Electronic Peak Flow MeterTaian Dalu Medical Instrument Co., Ltd.K222810TD-7301 Peak Flow meterGostar Co., Ltd.

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.

↑