FDA 510(k)

SL990, SL980, SL950

K-Number: K992836 · 1999-11-09

ApplicantCso

Decision Date1999-11-09

Product CodeHJO

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

SL990, SL980, SL950 is the device name listed in this FDA 510(k) record. The listed applicant is Cso. It received FDA 510(k) clearance on 1999-11-09 under 510(k) number K992836. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SL990, SL980, SL950?

SL990, SL980, SL950 is a medical device that received FDA 510(k) clearance on 1999-11-09. The listed applicant is Cso. The 510(k) number is K992836.

When did SL990, SL980, SL950 receive FDA 510(k) clearance?

SL990, SL980, SL950 received FDA 510(k) clearance on 1999-11-09, under 510(k) number K992836.

Who is the listed applicant for SL990, SL980, SL950?

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

What is the FDA product code for SL990, SL980, SL950?

The FDA product code for SL990, SL980, SL950 is HJO.

Other records listing Cso 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.

K992835C.S.O. TONOMETER

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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.