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)

SAFE-T-STIK

K-Number: K904382 · 1990-10-17

Decision Date1990-10-17
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFE-T-STIK is the device name listed in this FDA 510(k) record. The listed applicant is Xikon Technology. It received FDA 510(k) clearance on 1990-10-17 under 510(k) number K904382. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFE-T-STIK?

SAFE-T-STIK is a medical device that received FDA 510(k) clearance on 1990-10-17. The listed applicant is Xikon Technology. The 510(k) number is K904382.

When did SAFE-T-STIK receive FDA 510(k) clearance?

SAFE-T-STIK received FDA 510(k) clearance on 1990-10-17, under 510(k) number K904382.

Who is the listed applicant for SAFE-T-STIK?

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

What is the FDA product code for SAFE-T-STIK?

The FDA product code for SAFE-T-STIK is FMF.

Related Devices (Code: FMF)

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.

↑