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FDA 510(k)

RHYS-DAVIES EXSANGUINATOR

K-Number: K842963 · 1984-08-17

ApplicantWoodville Polymer Engineering, Ltd.
Decision Date1984-08-17
Product CodeKCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RHYS-DAVIES EXSANGUINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Woodville Polymer Engineering, Ltd.. It received FDA 510(k) clearance on 1984-08-17 under 510(k) number K842963. The device is classified under product code KCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHYS-DAVIES EXSANGUINATOR?

RHYS-DAVIES EXSANGUINATOR is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is Woodville Polymer Engineering, Ltd.. The 510(k) number is K842963.

When did RHYS-DAVIES EXSANGUINATOR receive FDA 510(k) clearance?

RHYS-DAVIES EXSANGUINATOR received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842963.

Who is the listed applicant for RHYS-DAVIES EXSANGUINATOR?

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

What is the FDA product code for RHYS-DAVIES EXSANGUINATOR?

The FDA product code for RHYS-DAVIES EXSANGUINATOR is KCY.

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Related Devices (Code: KCY)

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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