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FDA 510(k)

LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER

K-Number: K895718 · 1989-10-19

ApplicantData Medical Associates, Inc.
Decision Date1989-10-19
Product CodeJGM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Data Medical Associates, Inc.. It received FDA 510(k) clearance on 1989-10-19 under 510(k) number K895718. The device is classified under product code JGM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER?

LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER is a medical device that received FDA 510(k) clearance on 1989-10-19. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K895718.

When did LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER receive FDA 510(k) clearance?

LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER received FDA 510(k) clearance on 1989-10-19, under 510(k) number K895718.

Who is the listed applicant for LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER?

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

What is the FDA product code for LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER?

The FDA product code for LITHIUM CONCENTRATE FOR A FLAME PHOTOMETER is JGM.

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Other records listing Data Medical Associates, 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.

K993098HDL-C/LDL-C CALIBRATOR, MODEL 1913-003K971113DMA TRIGLYCERIDES PROCEDURESK961919DMA GAMMA GLUTAMYLTRANSFERASE (GGT) PROCEDUREK955796IRON CALIBRATOR & CALIBRATION VERIFICATION SETK955302SERUM BICARBONATE/CARBON DIOXIDEK955300TOTAL BILIRUBIN PROCEDURE

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Related Devices (Code: JGM)

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.

K862300AMRESCO FLOW PAC SODIUM POTASSIUM REAGENTAmresco, Inc.K831300MSI-NAK-50 TEST KITMedical Specialties, Inc.K810253SODIUM & POTASSIUM TEST KITMallinckrodt Critical CareK771068TRIGLYCERIDE KITEnvironmental Chemical Specialties

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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