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)

PRECI-JET 50

K-Number: K921797 · 1992-11-17

Decision Date1992-11-17
Product CodeKZE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRECI-JET 50 is the device name listed in this FDA 510(k) record. The listed applicant is Hmi Industries, Inc.. It received FDA 510(k) clearance on 1992-11-17 under 510(k) number K921797. The device is classified under product code KZE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECI-JET 50?

PRECI-JET 50 is a medical device that received FDA 510(k) clearance on 1992-11-17. The listed applicant is Hmi Industries, Inc.. The 510(k) number is K921797.

When did PRECI-JET 50 receive FDA 510(k) clearance?

PRECI-JET 50 received FDA 510(k) clearance on 1992-11-17, under 510(k) number K921797.

Who is the listed applicant for PRECI-JET 50?

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

What is the FDA product code for PRECI-JET 50?

The FDA product code for PRECI-JET 50 is KZE.

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 Hmi 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.

Related Devices (Code: KZE)

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.

↑