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FDA 510(k)

CARESIDE AMMONIA

K-Number: K991371 · 1999-08-03

ApplicantCareside, Inc.
Decision Date1999-08-03
Product CodeJID
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CARESIDE AMMONIA is the device name listed in this FDA 510(k) record. The listed applicant is Careside, Inc.. It received FDA 510(k) clearance on 1999-08-03 under 510(k) number K991371. The device is classified under product code JID. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARESIDE AMMONIA?

CARESIDE AMMONIA is a medical device that received FDA 510(k) clearance on 1999-08-03. The listed applicant is Careside, Inc.. The 510(k) number is K991371.

When did CARESIDE AMMONIA receive FDA 510(k) clearance?

CARESIDE AMMONIA received FDA 510(k) clearance on 1999-08-03, under 510(k) number K991371.

Who is the listed applicant for CARESIDE AMMONIA?

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

What is the FDA product code for CARESIDE AMMONIA?

The FDA product code for CARESIDE AMMONIA is JID.

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Other records listing Careside, 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.

K020484CARESIDE LDHK020486CARESIDE GGTK020487CARESIDE ALTK020488CARESIDE TRGLYCERIDEK002792CARESIDE CHOLINESTERASEK001462CARESIDE HEMOGLOBIN

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Related Devices (Code: JID)

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.

K260613AMI™ Plasma Cartridge, AMI™Sequitur Health Corp.K820723KODAK EKTACHEM CLINICAL CHEM. NH3Eastman Kodak CompanyK813366AMMONIA TESTWako Pure Chemical Industries, Ltd.

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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