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FDA 510(k)

ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE

K-Number: K940322 · 1994-11-28

Decision Date1994-11-28
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Arbo Medical, Inc.. It received FDA 510(k) clearance on 1994-11-28 under 510(k) number K940322. 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 ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE?

ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE is a medical device that received FDA 510(k) clearance on 1994-11-28. The listed applicant is Arbo Medical, Inc.. The 510(k) number is K940322.

When did ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE receive FDA 510(k) clearance?

ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE received FDA 510(k) clearance on 1994-11-28, under 510(k) number K940322.

Who is the listed applicant for ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE?

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

What is the FDA product code for ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE?

The FDA product code for ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE is DSA.

Related Clinical Trials

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Other records listing Arbo Medical, 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.

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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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