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)

VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER

K-Number: K120118 · 2012-05-24

ApplicantVentlab Corp.
Decision Date2012-05-24
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 2012-05-24 under 510(k) number K120118. The device is classified under product code CAP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER?

VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER is a medical device that received FDA 510(k) clearance on 2012-05-24. The listed applicant is Ventlab Corp.. The 510(k) number is K120118.

When did VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER receive FDA 510(k) clearance?

VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER received FDA 510(k) clearance on 2012-05-24, under 510(k) number K120118.

Who is the listed applicant for VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER?

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

What is the FDA product code for VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER?

The FDA product code for VENTLAB PRESSURECHEK DISOSABLE COLUMN MANOMETER is CAP.

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 Ventlab 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.

K102674CUFF SENTRYK093617VENTLAB 6000 SERIES HUMIDIFIERK093525ACE/STATCHECK II CO2 INDICATOR, ACE/STATCHECK II CO2 INDICATOR ARM ASSEMBY ADULT STATCHECK RESUSCITATOR WITH ACE/STATCHEK090840VENTLAB 5000 SERIES NEBULIZER ASSEMBLY, CUP, CUP W/ MASK, CUP W/ FITSALL CONN.K082204SERIES SY DISPOSABLE ELECTROSURGICAL PADK063813VENTLAB NASAL CO2 SAMPLING/O2 DELIVERY CANNULA

View all 22 devices →

Related Devices (Code: CAP)

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.

K201666SINGLE USE MANOMETERFlexicare Medical Limited.K182292VORTRAN APM-PlusVortran Medical Technology 1, Inc.K180510NS 120P-TRS Airway Pressure GaugeInstrumentation Industries, Inc.K172284NAPA LP-15 Airway Pressure MonitorDrw Medical, LLCK153733VORTRAN ManometerVortran Medical Technology 1, Inc.K122627GIO DIGITAL PRESSURE GUAGESGalemed Corp.

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.

↑