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FDA 510(k)

ACTA OEM MODULE

K-Number: K972006 · 1997-07-10

ApplicantInteractive Consulting, Inc.
Decision Date1997-07-10
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACTA OEM MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Interactive Consulting, Inc.. It received FDA 510(k) clearance on 1997-07-10 under 510(k) number K972006. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTA OEM MODULE?

ACTA OEM MODULE is a medical device that received FDA 510(k) clearance on 1997-07-10. The listed applicant is Interactive Consulting, Inc.. The 510(k) number is K972006.

When did ACTA OEM MODULE receive FDA 510(k) clearance?

ACTA OEM MODULE received FDA 510(k) clearance on 1997-07-10, under 510(k) number K972006.

Who is the listed applicant for ACTA OEM MODULE?

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

What is the FDA product code for ACTA OEM MODULE?

The FDA product code for ACTA OEM MODULE is EBZ.

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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.

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