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)

RELIANCE FAMILY OF WASHER-DISINFECTORS

K-Number: K983068 · 2000-05-31

Decision Date2000-05-31
Product CodeLDS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RELIANCE FAMILY OF WASHER-DISINFECTORS is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2000-05-31 under 510(k) number K983068. The device is classified under product code LDS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIANCE FAMILY OF WASHER-DISINFECTORS?

RELIANCE FAMILY OF WASHER-DISINFECTORS is a medical device that received FDA 510(k) clearance on 2000-05-31. The listed applicant is STERIS Corporation. The 510(k) number is K983068.

When did RELIANCE FAMILY OF WASHER-DISINFECTORS receive FDA 510(k) clearance?

RELIANCE FAMILY OF WASHER-DISINFECTORS received FDA 510(k) clearance on 2000-05-31, under 510(k) number K983068.

Who is the listed applicant for RELIANCE FAMILY OF WASHER-DISINFECTORS?

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

What is the FDA product code for RELIANCE FAMILY OF WASHER-DISINFECTORS?

The FDA product code for RELIANCE FAMILY OF WASHER-DISINFECTORS is LDS.

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 STERIS Corporation 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 196 devices →

Related Devices (Code: LDS)

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.

↑