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Variants of ACCUFLATE by Instrumed, Inc.
2 variants
Key
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Accuflate
Instrumed, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K910512
Active
Cleared 19 Feb 1991
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
I
Accuflate
Instrumed, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K924273
Active
Cleared 12 Jan 1993
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
I
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