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FDA 510(k)

PHAMAS ALLERGY MGMT. SYSTEM

K-Number: K841915 · 1984-05-09

ApplicantPharmacia, Inc.
Decision Date1984-05-09
Product Code
DecisionUnknown

Device Summary

PHAMAS ALLERGY MGMT. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1984-05-09 under 510(k) number K841915. FDA Decision: Unknown.

Frequently Asked Questions

What is the PHAMAS ALLERGY MGMT. SYSTEM?

PHAMAS ALLERGY MGMT. SYSTEM is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Pharmacia, Inc.. The 510(k) number is K841915.

When did PHAMAS ALLERGY MGMT. SYSTEM receive FDA 510(k) clearance?

PHAMAS ALLERGY MGMT. SYSTEM received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841915.

Who is the listed applicant for PHAMAS ALLERGY MGMT. SYSTEM?

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

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Other records listing Pharmacia, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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