FDA 510(k)

PATIENT GUIDED ELBOW & SHOULDER EXERC

K-Number: K830793 · 1983-06-16

Decision Date1983-06-16

Product CodeBXB

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

PATIENT GUIDED ELBOW & SHOULDER EXERC is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1983-06-16 under 510(k) number K830793. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT GUIDED ELBOW & SHOULDER EXERC?

PATIENT GUIDED ELBOW & SHOULDER EXERC is a medical device that received FDA 510(k) clearance on 1983-06-16. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K830793.

When did PATIENT GUIDED ELBOW & SHOULDER EXERC receive FDA 510(k) clearance?

PATIENT GUIDED ELBOW & SHOULDER EXERC received FDA 510(k) clearance on 1983-06-16, under 510(k) number K830793.

Who is the listed applicant for PATIENT GUIDED ELBOW & SHOULDER EXERC?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PATIENT GUIDED ELBOW & SHOULDER EXERC?

The FDA product code for PATIENT GUIDED ELBOW & SHOULDER EXERC is BXB.

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Other records listing Richard'S Medical Equip., Inc. as applicant

K823837RMC TOTAL KNEE SYSTEM K823724SPECTRON NECK REPLACEMENT PROSTHESIS K823726SPECTRON CONVERSION ENDOPROSTHESIS CUP K823723SPECTRON PROXIMAL FEMORAL PROSTHESIS K823722SPECTRON LONG, STRAIGHT FEMORAL PROSTHES K823727SPECTRON PRIMARY STEM FEMORAL PROSTHES

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Related Devices (Code: BXB)

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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.