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FDA 510(k)

DIAMOND MEDICAL, INC. MODEL DM 800

K-Number: K874709 · 1988-02-08

ApplicantDiamond Medical, Inc.
Decision Date1988-02-08
Product CodeFFT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIAMOND MEDICAL, INC. MODEL DM 800 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 1988-02-08 under 510(k) number K874709. The device is classified under product code FFT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAMOND MEDICAL, INC. MODEL DM 800?

DIAMOND MEDICAL, INC. MODEL DM 800 is a medical device that received FDA 510(k) clearance on 1988-02-08. The listed applicant is Diamond Medical, Inc.. The 510(k) number is K874709.

When did DIAMOND MEDICAL, INC. MODEL DM 800 receive FDA 510(k) clearance?

DIAMOND MEDICAL, INC. MODEL DM 800 received FDA 510(k) clearance on 1988-02-08, under 510(k) number K874709.

Who is the listed applicant for DIAMOND MEDICAL, INC. MODEL DM 800?

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 DIAMOND MEDICAL, INC. MODEL DM 800?

The FDA product code for DIAMOND MEDICAL, INC. MODEL DM 800 is FFT.

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/CARTRIDGEK915087DMI BLOD GAS ANALYZER/CARTRIDGEK874710DIAMOND MEDICAL, INC. MODEL DM 600K875369MODEL ISO-2001 UNIV. PATIENT ISOLATION CIRCUITK863298DIAMOND MEDICAL, INC., MODEL DM 700

Related Devices (Code: FFT)

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.

K102543BRAVO PH MONITORING SYSTEM AND ACCESSORIESGiven Imaging , Ltd.K013951SANDHILL SCIENTIFIC PEDIATEC PH PROBESandhill Scientific, Inc.K002028BRAVO PH MONITORING SYSTEMEndonetics, Inc.K961346PH ANALYSIS MODULESynectics-DantecK950087LOT 440Medical Instruments Corporation Mic AGK955018TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATORInstrumentarium Corp.

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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