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FDA 510(k)

SECHRIST AIRWAY PRESSURE MONITOR #400

K-Number: K810648 · 1981-03-20

ApplicantSechrist Industries, Inc.
Decision Date1981-03-20
Product CodeCAP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SECHRIST AIRWAY PRESSURE MONITOR #400 is the device name listed in this FDA 510(k) record. The listed applicant is Sechrist Industries, Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810648. 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 SECHRIST AIRWAY PRESSURE MONITOR #400?

SECHRIST AIRWAY PRESSURE MONITOR #400 is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Sechrist Industries, Inc.. The 510(k) number is K810648.

When did SECHRIST AIRWAY PRESSURE MONITOR #400 receive FDA 510(k) clearance?

SECHRIST AIRWAY PRESSURE MONITOR #400 received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810648.

Who is the listed applicant for SECHRIST AIRWAY PRESSURE MONITOR #400?

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

What is the FDA product code for SECHRIST AIRWAY PRESSURE MONITOR #400?

The FDA product code for SECHRIST AIRWAY PRESSURE MONITOR #400 is CAP.

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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 Sechrist Industries, 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.

K100268SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBERK052713MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBERK023745SECHRIST AIR/OXYGEN MIXER, MODEL 3500 CP-GK993167MILLENNIUM INFANT VENTILATORK992503SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIESK950386MODEL 3200P/3200PR HYPERBARIC CHAMBER

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.

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