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Variants of IQ SYSTEM by Renaissance Technology, Inc.
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Iq System
Renaissance Technology, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K981720
Active
Cleared 8 Feb 1999
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Iq System
Renaissance Technology, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K922218
Active
Cleared 8 Dec 1992
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
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