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)

STATClave G4 Chamber Autoclave

K-Number: K192910 · 2020-06-19

ApplicantScican , Ltd.
Decision Date2020-06-19
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STATClave G4 Chamber Autoclave is the device name listed in this FDA 510(k) record. The listed applicant is Scican , Ltd.. It received FDA 510(k) clearance on 2020-06-19 under 510(k) number K192910. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STATClave G4 Chamber Autoclave?

STATClave G4 Chamber Autoclave is a medical device that received FDA 510(k) clearance on 2020-06-19. The listed applicant is Scican , Ltd.. The 510(k) number is K192910.

When did STATClave G4 Chamber Autoclave receive FDA 510(k) clearance?

STATClave G4 Chamber Autoclave received FDA 510(k) clearance on 2020-06-19, under 510(k) number K192910.

Who is the listed applicant for STATClave G4 Chamber Autoclave?

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

What is the FDA product code for STATClave G4 Chamber Autoclave?

The FDA product code for STATClave G4 Chamber Autoclave is FLE.

Other records listing Scican , Ltd. 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: FLE)

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.