FDA 510(k)

BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000

K-Number: K010809 · 2001-05-23

Decision Date2001-05-23

Product CodeDSA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000 is the device name listed in this FDA 510(k) record. The listed applicant is Rf Industries, Ltd.. It received FDA 510(k) clearance on 2001-05-23 under 510(k) number K010809. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000?

BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000 is a medical device that received FDA 510(k) clearance on 2001-05-23. The listed applicant is Rf Industries, Ltd.. The 510(k) number is K010809.

When did BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000 receive FDA 510(k) clearance?

BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000 received FDA 510(k) clearance on 2001-05-23, under 510(k) number K010809.

Who is the listed applicant for BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000?

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

What is the FDA product code for BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000?

The FDA product code for BIOCONNECT PATIENT MONITORING CABLES AND LEADWIRES, CAT# 1000 THRU CAT# 40000 is DSA.

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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.