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FDA 510(k)

MULTI DOPPLEX, MD-1

K-Number: K900882 · 1990-08-22

ApplicantHuntleigh Technology, Inc.
Decision Date1990-08-22
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTI DOPPLEX, MD-1 is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1990-08-22 under 510(k) number K900882. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI DOPPLEX, MD-1?

MULTI DOPPLEX, MD-1 is a medical device that received FDA 510(k) clearance on 1990-08-22. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K900882.

When did MULTI DOPPLEX, MD-1 receive FDA 510(k) clearance?

MULTI DOPPLEX, MD-1 received FDA 510(k) clearance on 1990-08-22, under 510(k) number K900882.

Who is the listed applicant for MULTI DOPPLEX, MD-1?

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

What is the FDA product code for MULTI DOPPLEX, MD-1?

The FDA product code for MULTI DOPPLEX, MD-1 is JAF.

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Other records listing Huntleigh Technology, 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.

K992733AKRON ATP9 TRACTION MACHINEK964699RHEO DOPPLEX II (RD 2)K924516OP3/VP4K910188FLOWPLUS AC330 PUMP GARMENTSK900618HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140K890012HUNTLEIGH DYNAMIC FLOTATION SYSTEM

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Related Devices (Code: JAF)

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.

K242487Laminar P1 (LDH-HW-001)Laminar Digital Health, Inc.K110628SIMPLEABINewman MedicalK093393LIFEDOP MODEL 300ABISummit Doppler Systems, Inc.K090009THD SLIDE ONEThd SpaK081429THD SLIDEThd SpaK070815THDG.F. S.R.L.

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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