FDA 510(k)

SCANNER, CT, 0400

K-Number: K772289 · 1977-12-21

Decision Date1977-12-21

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SCANNER, CT, 0400 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 1977-12-21 under 510(k) number K772289. 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 SCANNER, CT, 0400?

SCANNER, CT, 0400 is a medical device that received FDA 510(k) clearance on 1977-12-21. The listed applicant is Pfizer Medical Systems, Inc.. The 510(k) number is K772289.

When did SCANNER, CT, 0400 receive FDA 510(k) clearance?

SCANNER, CT, 0400 received FDA 510(k) clearance on 1977-12-21, under 510(k) number K772289.

Who is the listed applicant for SCANNER, CT, 0400?

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 SCANNER, CT, 0400?

The FDA product code for SCANNER, CT, 0400 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.