Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PHADEBACT SHIGELLA TEST

K-Number: K880752 · 1989-02-17

ApplicantPharmacia, Inc.
Decision Date1989-02-17
Product CodeGNB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PHADEBACT SHIGELLA TEST is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1989-02-17 under 510(k) number K880752. The device is classified under product code GNB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHADEBACT SHIGELLA TEST?

PHADEBACT SHIGELLA TEST is a medical device that received FDA 510(k) clearance on 1989-02-17. The listed applicant is Pharmacia, Inc.. The 510(k) number is K880752.

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

PHADEBACT SHIGELLA TEST received FDA 510(k) clearance on 1989-02-17, under 510(k) number K880752.

Who is the listed applicant for PHADEBACT SHIGELLA TEST?

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 SHIGELLA TEST?

The FDA product code for PHADEBACT SHIGELLA TEST is GNB.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 129 devices →

Related Devices (Code: GNB)

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.

K961537SAS SHIGELLA SONNEI FORM II ANTISERUMSa Scientific, Inc.K961549SAS SHIGELLA FLEXNERI TYPE 2 ANTISERUMSa Scientific, Inc.K961535SAS SHIGELLA DYSENTERIAE GROUP A1 (8-10) ANTISERUMSa Scientific, Inc.K961534SAS SHIGELLA SONNEI FORM I ANTISERUM (3/100/1000ML)Sa Scientific, Inc.K961553SAS SHIGELLA DYSENTERIAE TYPE 1 ANTISERUMSa Scientific, Inc.K961540SAS SHIGELLA SONNEI GROUP D ANTISERUMSa Scientific, Inc.

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.

↑