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FDA 510(k)

ABUSCREEN(R) ONLINE CONTROLS

K-Number: K910689 · 1991-03-11

Decision Date1991-03-11
Product CodeLAS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ABUSCREEN(R) ONLINE CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1991-03-11 under 510(k) number K910689. The device is classified under product code LAS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABUSCREEN(R) ONLINE CONTROLS?

ABUSCREEN(R) ONLINE CONTROLS is a medical device that received FDA 510(k) clearance on 1991-03-11. The listed applicant is Roche Diagnostic Systems, Inc.. The 510(k) number is K910689.

When did ABUSCREEN(R) ONLINE CONTROLS receive FDA 510(k) clearance?

ABUSCREEN(R) ONLINE CONTROLS received FDA 510(k) clearance on 1991-03-11, under 510(k) number K910689.

Who is the listed applicant for ABUSCREEN(R) ONLINE CONTROLS?

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

What is the FDA product code for ABUSCREEN(R) ONLINE CONTROLS?

The FDA product code for ABUSCREEN(R) ONLINE CONTROLS is LAS.

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 Roche Diagnostic 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 296 devices →

Related Devices (Code: LAS)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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