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FDA 510(k)

PAIN CARE MULTI-PORT CATHETER, MODEL 2000L

K-Number: K003611 · 2000-12-13

ApplicantBreg, Inc.
Decision Date2000-12-13
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PAIN CARE MULTI-PORT CATHETER, MODEL 2000L is the device name listed in this FDA 510(k) record. The listed applicant is Breg, Inc.. It received FDA 510(k) clearance on 2000-12-13 under 510(k) number K003611. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAIN CARE MULTI-PORT CATHETER, MODEL 2000L?

PAIN CARE MULTI-PORT CATHETER, MODEL 2000L is a medical device that received FDA 510(k) clearance on 2000-12-13. The listed applicant is Breg, Inc.. The 510(k) number is K003611.

When did PAIN CARE MULTI-PORT CATHETER, MODEL 2000L receive FDA 510(k) clearance?

PAIN CARE MULTI-PORT CATHETER, MODEL 2000L received FDA 510(k) clearance on 2000-12-13, under 510(k) number K003611.

Who is the listed applicant for PAIN CARE MULTI-PORT CATHETER, MODEL 2000L?

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

What is the FDA product code for PAIN CARE MULTI-PORT CATHETER, MODEL 2000L?

The FDA product code for PAIN CARE MULTI-PORT CATHETER, MODEL 2000L is FRN.

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Other records listing Breg, Inc. as applicant

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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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