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FDA 510(k)

PHADEBASE HUMYLASE CONTROL

K-Number: K822938 · 1982-11-05

ApplicantPharmacia, Inc.
Decision Date1982-11-05
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHADEBASE HUMYLASE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1982-11-05 under 510(k) number K822938. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHADEBASE HUMYLASE CONTROL?

PHADEBASE HUMYLASE CONTROL is a medical device that received FDA 510(k) clearance on 1982-11-05. The listed applicant is Pharmacia, Inc.. The 510(k) number is K822938.

When did PHADEBASE HUMYLASE CONTROL receive FDA 510(k) clearance?

PHADEBASE HUMYLASE CONTROL received FDA 510(k) clearance on 1982-11-05, under 510(k) number K822938.

Who is the listed applicant for PHADEBASE HUMYLASE CONTROL?

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 PHADEBASE HUMYLASE CONTROL?

The FDA product code for PHADEBASE HUMYLASE CONTROL is JJX.

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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

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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