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FDA 510(k)

ACTA-SCANNER R 0200FS

K-Number: K770573 · 1977-03-30

ApplicantPfizer Medical Systems, Inc.
Decision Date1977-03-30
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACTA-SCANNER R 0200FS is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer Medical Systems, Inc.. It received FDA 510(k) clearance on 1977-03-30 under 510(k) number K770573. 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 R 0200FS?

ACTA-SCANNER R 0200FS is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is Pfizer Medical Systems, Inc.. The 510(k) number is K770573.

When did ACTA-SCANNER R 0200FS receive FDA 510(k) clearance?

ACTA-SCANNER R 0200FS received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770573.

Who is the listed applicant for ACTA-SCANNER R 0200FS?

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

What is the FDA product code for ACTA-SCANNER R 0200FS?

The FDA product code for ACTA-SCANNER R 0200FS is JAK.

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Other records listing Pfizer Medical Systems, Inc. as applicant

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Related Devices (Code: 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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