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FDA 510(k)

JRP Wound Spreader

K-Number: K152538 · 2016-04-13

ApplicantJ.R. Parker, LLC
Decision Date2016-04-13
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

JRP Wound Spreader is the device name listed in this FDA 510(k) record. The listed applicant is J.R. Parker, LLC. It received FDA 510(k) clearance on 2016-04-13 under 510(k) number K152538. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JRP Wound Spreader?

JRP Wound Spreader is a medical device that received FDA 510(k) clearance on 2016-04-13. The listed applicant is J.R. Parker, LLC. The 510(k) number is K152538.

When did JRP Wound Spreader receive FDA 510(k) clearance?

JRP Wound Spreader received FDA 510(k) clearance on 2016-04-13, under 510(k) number K152538.

Who is the listed applicant for JRP Wound Spreader?

The FDA 510(k) record lists J.R. Parker, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JRP Wound Spreader?

The FDA product code for JRP Wound Spreader is GAD.

Related Devices (Code: GAD)

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.

K151104OTELO LLSpineart

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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