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FDA 510(k)

DIRECTOR

K-Number: K832658 · 1983-10-04

ApplicantPharmacia, Inc.
Decision Date1983-10-04
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIRECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832658. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIRECTOR?

DIRECTOR is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Pharmacia, Inc.. The 510(k) number is K832658.

When did DIRECTOR receive FDA 510(k) clearance?

DIRECTOR received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832658.

Who is the listed applicant for DIRECTOR?

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 DIRECTOR?

The FDA product code for DIRECTOR is FMF.

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Other records listing Pharmacia, Inc. as applicant

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K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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Related Devices (Code: FMF)

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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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