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)

MUMPS COMPLEMENT FIXATION & HEMAGGLU

K-Number: K832873 · 1983-12-27

ApplicantHazleton Dutchland, Inc.
Decision Date1983-12-27
Product CodeGRC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUMPS COMPLEMENT FIXATION & HEMAGGLU is the device name listed in this FDA 510(k) record. The listed applicant is Hazleton Dutchland, Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K832873. The device is classified under product code GRC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUMPS COMPLEMENT FIXATION & HEMAGGLU?

MUMPS COMPLEMENT FIXATION & HEMAGGLU is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Hazleton Dutchland, Inc.. The 510(k) number is K832873.

When did MUMPS COMPLEMENT FIXATION & HEMAGGLU receive FDA 510(k) clearance?

MUMPS COMPLEMENT FIXATION & HEMAGGLU received FDA 510(k) clearance on 1983-12-27, under 510(k) number K832873.

Who is the listed applicant for MUMPS COMPLEMENT FIXATION & HEMAGGLU?

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

What is the FDA product code for MUMPS COMPLEMENT FIXATION & HEMAGGLU?

The FDA product code for MUMPS COMPLEMENT FIXATION & HEMAGGLU is GRC.

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

Related Devices (Code: GRC)

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.

K905306MUMPS COMPLEMENT-FIXATION (C.F.) ANTIGENVirion (U.S.), Inc.K802933MUMPS S & V ANTIGENS & CONTROLSOrion Diagnostica, 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.

↑