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)

SECHRIST MODEL 990 JET VENTILATOR

K-Number: K821930 · 1982-08-16

Decision Date1982-08-16
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SECHRIST MODEL 990 JET VENTILATOR 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 1982-08-16 under 510(k) number K821930. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SECHRIST MODEL 990 JET VENTILATOR?

SECHRIST MODEL 990 JET VENTILATOR is a medical device that received FDA 510(k) clearance on 1982-08-16. The listed applicant is Sechrist Industries, Inc.. The 510(k) number is K821930.

When did SECHRIST MODEL 990 JET VENTILATOR receive FDA 510(k) clearance?

SECHRIST MODEL 990 JET VENTILATOR received FDA 510(k) clearance on 1982-08-16, under 510(k) number K821930.

Who is the listed applicant for SECHRIST MODEL 990 JET VENTILATOR?

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 MODEL 990 JET VENTILATOR?

The FDA product code for SECHRIST MODEL 990 JET VENTILATOR is CBK.

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.

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.

View all 22 devices →

Related Devices (Code: CBK)

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.

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.

↑