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FDA 510(k)

ELECTROLYTE ANALYZER SERA-252

K-Number: K853405 · 1985-12-04

ApplicantHoriba Instruments, Inc.
Decision Date1985-12-04
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTROLYTE ANALYZER SERA-252 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 1985-12-04 under 510(k) number K853405. The device is classified under product code CHL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROLYTE ANALYZER SERA-252?

ELECTROLYTE ANALYZER SERA-252 is a medical device that received FDA 510(k) clearance on 1985-12-04. The listed applicant is Horiba Instruments, Inc.. The 510(k) number is K853405.

When did ELECTROLYTE ANALYZER SERA-252 receive FDA 510(k) clearance?

ELECTROLYTE ANALYZER SERA-252 received FDA 510(k) clearance on 1985-12-04, under 510(k) number K853405.

Who is the listed applicant for ELECTROLYTE ANALYZER SERA-252?

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

What is the FDA product code for ELECTROLYTE ANALYZER SERA-252?

The FDA product code for ELECTROLYTE ANALYZER SERA-252 is CHL.

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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.

K853356SERA-210 ELECTROLYTE ANALYZERK844806MODIFY ELECTROLYTE ANALYZER MODEL SERA-210K841424ELECTROLYTE ANALYZER SERA-210K841441SERA-250

Related Devices (Code: CHL)

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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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