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FDA 510(k)

ACTA-SCANNER 0220FS

K-Number: K791153 · 1979-08-03

ApplicantPfizer, Inc.
Decision Date1979-08-03
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACTA-SCANNER 0220FS is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer, Inc.. It received FDA 510(k) clearance on 1979-08-03 under 510(k) number K791153. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTA-SCANNER 0220FS?

ACTA-SCANNER 0220FS is a medical device that received FDA 510(k) clearance on 1979-08-03. The listed applicant is Pfizer, Inc.. The 510(k) number is K791153.

When did ACTA-SCANNER 0220FS receive FDA 510(k) clearance?

ACTA-SCANNER 0220FS received FDA 510(k) clearance on 1979-08-03, under 510(k) number K791153.

Who is the listed applicant for ACTA-SCANNER 0220FS?

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

What is the FDA product code for ACTA-SCANNER 0220FS?

The FDA product code for ACTA-SCANNER 0220FS is JAK.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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