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FDA 510(k)

DMI BLOD GAS ANALYZER/CARTRIDGE

K-Number: K915087 · 1992-01-08

ApplicantDiamond Medical, Inc.
Decision Date1992-01-08
Product CodeCHL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DMI BLOD GAS ANALYZER/CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Diamond Medical, Inc.. It received FDA 510(k) clearance on 1992-01-08 under 510(k) number K915087. 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 DMI BLOD GAS ANALYZER/CARTRIDGE?

DMI BLOD GAS ANALYZER/CARTRIDGE is a medical device that received FDA 510(k) clearance on 1992-01-08. The listed applicant is Diamond Medical, Inc.. The 510(k) number is K915087.

When did DMI BLOD GAS ANALYZER/CARTRIDGE receive FDA 510(k) clearance?

DMI BLOD GAS ANALYZER/CARTRIDGE received FDA 510(k) clearance on 1992-01-08, under 510(k) number K915087.

Who is the listed applicant for DMI BLOD GAS ANALYZER/CARTRIDGE?

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

What is the FDA product code for DMI BLOD GAS ANALYZER/CARTRIDGE?

The FDA product code for DMI BLOD GAS ANALYZER/CARTRIDGE is CHL.

Related Clinical Trials

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.

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Other records listing Diamond Medical, 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.

K924758DMI BLOOD GAS ANALYZER/CARTRIDGEK874709DIAMOND MEDICAL, INC. MODEL DM 800K874710DIAMOND MEDICAL, INC. MODEL DM 600K875369MODEL ISO-2001 UNIV. PATIENT ISOLATION CIRCUITK863298DIAMOND MEDICAL, INC., MODEL DM 700

Related Devices (Code: CHL)

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.

K252207ABL90 FLEX PLUS System, safeCLINITUBESRadiometer Medicals ApsK244014i-STAT CG4+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K240998ABL90 FLEX PLUS SystemRadiometer Medicals ApsK230285i-STAT CG8+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.K221900Stat Profile Prime Plus Analyzer SystemNova Biomedical CorporationK223857i-STAT G3+ cartridge with the i-STAT 1 SystemAbbott Point of Care, Inc.

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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