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)

LX 300 TISSUE PROCESSOR

K-Number: K853938 · 1985-10-10

Decision Date1985-10-10
Product CodeIEO
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

LX 300 TISSUE PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Systems, Inc.. It received FDA 510(k) clearance on 1985-10-10 under 510(k) number K853938. The device is classified under product code IEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LX 300 TISSUE PROCESSOR?

LX 300 TISSUE PROCESSOR is a medical device that received FDA 510(k) clearance on 1985-10-10. The listed applicant is Innovative Medical Systems, Inc.. The 510(k) number is K853938.

When did LX 300 TISSUE PROCESSOR receive FDA 510(k) clearance?

LX 300 TISSUE PROCESSOR received FDA 510(k) clearance on 1985-10-10, under 510(k) number K853938.

Who is the listed applicant for LX 300 TISSUE PROCESSOR?

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

What is the FDA product code for LX 300 TISSUE PROCESSOR?

The FDA product code for LX 300 TISSUE PROCESSOR is IEO.

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 Innovative Medical Systems, 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: IEO)

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.

↑