LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)
K-Number: K883599 · 1988-09-02
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Device Summary
Frequently Asked Questions
What is the LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)?
LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC) is a medical device that received FDA 510(k) clearance on 1988-09-02. The listed applicant is Innovative Medical Systems, Inc.. The 510(k) number is K883599.
When did LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC) receive FDA 510(k) clearance?
LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC) received FDA 510(k) clearance on 1988-09-02, under 510(k) number K883599.
Who is the listed applicant for LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)?
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-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)?
The FDA product code for LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC) 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.
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.
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