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FDA 510(k)

SECHRIST VOLUME VENTILATOR MODIFICATION

K-Number: K850740 · 1985-07-29

ApplicantSechrist Industries, Inc.
Decision Date1985-07-29
Product Code
DecisionSubstantially Equivalent

Device Summary

SECHRIST VOLUME VENTILATOR MODIFICATION 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 1985-07-29 under 510(k) number K850740. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECHRIST VOLUME VENTILATOR MODIFICATION?

SECHRIST VOLUME VENTILATOR MODIFICATION is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is Sechrist Industries, Inc.. The 510(k) number is K850740.

When did SECHRIST VOLUME VENTILATOR MODIFICATION receive FDA 510(k) clearance?

SECHRIST VOLUME VENTILATOR MODIFICATION received FDA 510(k) clearance on 1985-07-29, under 510(k) number K850740.

Who is the listed applicant for SECHRIST VOLUME VENTILATOR MODIFICATION?

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

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.

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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 SERIESK934164MODEL 2500E/2500ER HYPERBARIC CHAMBER

View all 22 devices →

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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