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FDA 510(k)

R&D RET-LINE KIT

K-Number: K013898 · 2002-01-22

Decision Date2002-01-22
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

R&D RET-LINE KIT is the device name listed in this FDA 510(k) record. The listed applicant is R&D Systems, Inc.. It received FDA 510(k) clearance on 2002-01-22 under 510(k) number K013898. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R&D RET-LINE KIT?

R&D RET-LINE KIT is a medical device that received FDA 510(k) clearance on 2002-01-22. The listed applicant is R&D Systems, Inc.. The 510(k) number is K013898.

When did R&D RET-LINE KIT receive FDA 510(k) clearance?

R&D RET-LINE KIT received FDA 510(k) clearance on 2002-01-22, under 510(k) number K013898.

Who is the listed applicant for R&D RET-LINE KIT?

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

What is the FDA product code for R&D RET-LINE KIT?

The FDA product code for R&D RET-LINE KIT is JPK.

Other records listing R&D Systems, 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.

View all 79 devices →

Related Devices (Code: JPK)

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.

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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