FDA 510(k)

THIGH HOLDER

K-Number: K832000 · 1983-07-12

Decision Date1983-07-12

Product Code

DecisionSubstantially Equivalent

Device Summary

THIGH HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Richards Manufacturer Co.. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K832000. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THIGH HOLDER?

THIGH HOLDER is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Richards Manufacturer Co.. The 510(k) number is K832000.

When did THIGH HOLDER receive FDA 510(k) clearance?

THIGH HOLDER received FDA 510(k) clearance on 1983-07-12, under 510(k) number K832000.

Who is the listed applicant for THIGH HOLDER?

The FDA 510(k) record lists Richards Manufacturer Co. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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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Other records listing Richards Manufacturer Co. as applicant

K831999FEMORAL CANAL SUCTION TAMPON K831884SPECTRON EXTRA-SMALL, STRAIGHT FEMORAL K831656ARTHROSCOPY KNIVES/PROBES/BENDING TOOL

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.