FDA 510(k)

FITO DIDO

K-Number: K963075 · 1996-08-22

Decision Date1996-08-22

Product CodeHQY

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

FITO DIDO is the device name listed in this FDA 510(k) record. The listed applicant is Framesmart, Inc.. It received FDA 510(k) clearance on 1996-08-22 under 510(k) number K963075. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FITO DIDO?

FITO DIDO is a medical device that received FDA 510(k) clearance on 1996-08-22. The listed applicant is Framesmart, Inc.. The 510(k) number is K963075.

When did FITO DIDO receive FDA 510(k) clearance?

FITO DIDO received FDA 510(k) clearance on 1996-08-22, under 510(k) number K963075.

Who is the listed applicant for FITO DIDO?

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

What is the FDA product code for FITO DIDO?

The FDA product code for FITO DIDO is HQY.

Other records listing Framesmart, 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.

K962912MARCELLA CARAN

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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.