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FDA 510(k)

PHADEBACT CSF TEST 20

K-Number: K822810 · 1982-12-30

ApplicantPharmacia, Inc.
Decision Date1982-12-30
Product CodeGTJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PHADEBACT CSF TEST 20 is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K822810. The device is classified under product code GTJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHADEBACT CSF TEST 20?

PHADEBACT CSF TEST 20 is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Pharmacia, Inc.. The 510(k) number is K822810.

When did PHADEBACT CSF TEST 20 receive FDA 510(k) clearance?

PHADEBACT CSF TEST 20 received FDA 510(k) clearance on 1982-12-30, under 510(k) number K822810.

Who is the listed applicant for PHADEBACT CSF TEST 20?

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

What is the FDA product code for PHADEBACT CSF TEST 20?

The FDA product code for PHADEBACT CSF TEST 20 is GTJ.

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Other records listing Pharmacia, Inc. as applicant

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Related Devices (Code: GTJ)

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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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