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FDA 510(k)

DIAG. CONSOLE, INDEPENDENT

K-Number: K772291 · 1977-12-21

ApplicantPfizer, Inc.
Decision Date1977-12-21
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAG. CONSOLE, INDEPENDENT is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer, Inc.. It received FDA 510(k) clearance on 1977-12-21 under 510(k) number K772291. 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 DIAG. CONSOLE, INDEPENDENT?

DIAG. CONSOLE, INDEPENDENT is a medical device that received FDA 510(k) clearance on 1977-12-21. The listed applicant is Pfizer, Inc.. The 510(k) number is K772291.

When did DIAG. CONSOLE, INDEPENDENT receive FDA 510(k) clearance?

DIAG. CONSOLE, INDEPENDENT received FDA 510(k) clearance on 1977-12-21, under 510(k) number K772291.

Who is the listed applicant for DIAG. CONSOLE, INDEPENDENT?

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 DIAG. CONSOLE, INDEPENDENT?

The FDA product code for DIAG. CONSOLE, INDEPENDENT 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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