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)

SERA-250

K-Number: K841441 · 1984-04-06

ApplicantHoriba Instruments, Inc.
Decision Date1984-04-06
Product Code
DecisionUnknown

Device Summary

SERA-250 is the device name listed in this FDA 510(k) record. The listed applicant is Horiba Instruments, Inc.. It received FDA 510(k) clearance on 1984-04-06 under 510(k) number K841441. FDA Decision: Unknown.

Frequently Asked Questions

What is the SERA-250?

SERA-250 is a medical device that received FDA 510(k) clearance on 1984-04-06. The listed applicant is Horiba Instruments, Inc.. The 510(k) number is K841441.

When did SERA-250 receive FDA 510(k) clearance?

SERA-250 received FDA 510(k) clearance on 1984-04-06, under 510(k) number K841441.

Who is the listed applicant for SERA-250?

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

Other records listing Horiba Instruments, 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.

K853405ELECTROLYTE ANALYZER SERA-252K853356SERA-210 ELECTROLYTE ANALYZERK844806MODIFY ELECTROLYTE ANALYZER MODEL SERA-210K841424ELECTROLYTE ANALYZER SERA-210

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.

↑