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FDA 510(k)

KODAK EKTACHEM CLINICAL CHEM. NH3

K-Number: K820723 · 1982-04-01

ApplicantEastman Kodak Company
Decision Date1982-04-01
Product CodeJID
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KODAK EKTACHEM CLINICAL CHEM. NH3 is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1982-04-01 under 510(k) number K820723. 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 KODAK EKTACHEM CLINICAL CHEM. NH3?

KODAK EKTACHEM CLINICAL CHEM. NH3 is a medical device that received FDA 510(k) clearance on 1982-04-01. The listed applicant is Eastman Kodak Company. The 510(k) number is K820723.

When did KODAK EKTACHEM CLINICAL CHEM. NH3 receive FDA 510(k) clearance?

KODAK EKTACHEM CLINICAL CHEM. NH3 received FDA 510(k) clearance on 1982-04-01, under 510(k) number K820723.

Who is the listed applicant for KODAK EKTACHEM CLINICAL CHEM. NH3?

The FDA 510(k) record lists Eastman Kodak Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KODAK EKTACHEM CLINICAL CHEM. NH3?

The FDA product code for KODAK EKTACHEM CLINICAL CHEM. NH3 is JID.

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Other records listing Eastman Kodak Company 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.

K060550KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386K060137KODAK ECLIPSE IMAGE PROCESSING SOFTWAREK060079KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEMK060055KODAK PACSK053347KODAK CARESTREAM PACSK051483KODAK DIRECTVIEW DR SYSTEM DETECTOR

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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.K991371CARESIDE AMMONIACareside, Inc.K813366AMMONIA 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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