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FDA 510(k)

PHADEBAS HUMYLASE CONTROL(H)

K-Number: K823421 · 1983-04-05

ApplicantPharmacia, Inc.
Decision Date1983-04-05
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHADEBAS HUMYLASE CONTROL(H) is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1983-04-05 under 510(k) number K823421. 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 PHADEBAS HUMYLASE CONTROL(H)?

PHADEBAS HUMYLASE CONTROL(H) is a medical device that received FDA 510(k) clearance on 1983-04-05. The listed applicant is Pharmacia, Inc.. The 510(k) number is K823421.

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

PHADEBAS HUMYLASE CONTROL(H) received FDA 510(k) clearance on 1983-04-05, under 510(k) number K823421.

Who is the listed applicant for PHADEBAS HUMYLASE CONTROL(H)?

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 PHADEBAS HUMYLASE CONTROL(H)?

The FDA product code for PHADEBAS HUMYLASE CONTROL(H) 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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