FDA 510(k)

HOLDSTER ARM RETENTION SYSTEM

K-Number: K844157 · 1985-01-23

Decision Date1985-01-23

Product Code

DecisionSubstantially Equivalent

Device Summary

HOLDSTER ARM RETENTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is P.G.L. Medical. It received FDA 510(k) clearance on 1985-01-23 under 510(k) number K844157. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLDSTER ARM RETENTION SYSTEM?

HOLDSTER ARM RETENTION SYSTEM is a medical device that received FDA 510(k) clearance on 1985-01-23. The listed applicant is P.G.L. Medical. The 510(k) number is K844157.

When did HOLDSTER ARM RETENTION SYSTEM receive FDA 510(k) clearance?

HOLDSTER ARM RETENTION SYSTEM received FDA 510(k) clearance on 1985-01-23, under 510(k) number K844157.

Who is the listed applicant for HOLDSTER ARM RETENTION SYSTEM?

The FDA 510(k) record lists P.G.L. Medical as the applicant. This does not by itself establish the device manufacturer.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.