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FDA 510(k)

ULTRA PVD

K-Number: K912925 · 1992-06-18

ApplicantAdvanced Medical Products, Inc.
Decision Date1992-06-18
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRA PVD is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Products, Inc.. It received FDA 510(k) clearance on 1992-06-18 under 510(k) number K912925. 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 ULTRA PVD?

ULTRA PVD is a medical device that received FDA 510(k) clearance on 1992-06-18. The listed applicant is Advanced Medical Products, Inc.. The 510(k) number is K912925.

When did ULTRA PVD receive FDA 510(k) clearance?

ULTRA PVD received FDA 510(k) clearance on 1992-06-18, under 510(k) number K912925.

Who is the listed applicant for ULTRA PVD?

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

What is the FDA product code for ULTRA PVD?

The FDA product code for ULTRA PVD is JAF.

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Other records listing Advanced Medical Products, 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.

K000932ARACHNOPHLEBECTOMY NEEDLEK923995URODYNAMICS TUBING KITS #5161, #5150, #7170K921426ULTRA PCIK915658SPECTRA ECGK896103MICRO FL 7400 AMBULATORY HOLTER/BP MONITORK896102MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR

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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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