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FDA 510(k)

ANGIOSCAN FLO MAD SPECTRUM ANALYZER

K-Number: K834525 · 1984-05-23

ApplicantUnigon Industries, Inc.
Decision Date1984-05-23
Product CodeJOP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIOSCAN FLO MAD SPECTRUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Unigon Industries, Inc.. It received FDA 510(k) clearance on 1984-05-23 under 510(k) number K834525. The device is classified under product code JOP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOSCAN FLO MAD SPECTRUM ANALYZER?

ANGIOSCAN FLO MAD SPECTRUM ANALYZER is a medical device that received FDA 510(k) clearance on 1984-05-23. The listed applicant is Unigon Industries, Inc.. The 510(k) number is K834525.

When did ANGIOSCAN FLO MAD SPECTRUM ANALYZER receive FDA 510(k) clearance?

ANGIOSCAN FLO MAD SPECTRUM ANALYZER received FDA 510(k) clearance on 1984-05-23, under 510(k) number K834525.

Who is the listed applicant for ANGIOSCAN FLO MAD SPECTRUM ANALYZER?

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

What is the FDA product code for ANGIOSCAN FLO MAD SPECTRUM ANALYZER?

The FDA product code for ANGIOSCAN FLO MAD SPECTRUM ANALYZER is JOP.

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 Unigon Industries, 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.

K834501ANGIOSCANE SPECTRUM ANALYZERK812184ANGIOSCAN SPECTRUM ANALYZER

Related Devices (Code: JOP)

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.

K242662Falcon/Xpress (Falcon/Xpress)Viasonix , Ltd.K233976VasoGuard (V10, V8, V6, V4, V2)Corvascular Diagnostics, LLCK153762Smartdop XT6Koven Technology, Inc.K131860VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDINGUs Vascular, LLCK111416FALCONViasonix , Ltd.K071730STUDIODOP VICORDERSkidmore Medical, Limited

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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