FDA 510(k)

VF-PD-120

K-Number: K842460 · 1984-10-19

Decision Date1984-10-19

Product CodeJOP

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

VF-PD-120 is the device name listed in this FDA 510(k) record. The listed applicant is Valpey-Fisher Corp.. It received FDA 510(k) clearance on 1984-10-19 under 510(k) number K842460. 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 VF-PD-120?

VF-PD-120 is a medical device that received FDA 510(k) clearance on 1984-10-19. The listed applicant is Valpey-Fisher Corp.. The 510(k) number is K842460.

When did VF-PD-120 receive FDA 510(k) clearance?

VF-PD-120 received FDA 510(k) clearance on 1984-10-19, under 510(k) number K842460.

Who is the listed applicant for VF-PD-120?

The FDA 510(k) record lists Valpey-Fisher Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VF-PD-120?

The FDA product code for VF-PD-120 is JOP.

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, LLC K153762Smartdop XT6Koven Technology, Inc.K131860VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDINGUs Vascular, LLC K111416FALCONViasonix , Ltd.K071730STUDIODOP VICORDERSkidmore Medical, Limited

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.