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FDA 510(k)

REM500 THREE WHEELED ELEC. CART.

K-Number: K872518 · 1987-07-28

ApplicantRoyal Enterprises Manufacturing, Inc.
Decision Date1987-07-28
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

REM500 THREE WHEELED ELEC. CART. is the device name listed in this FDA 510(k) record. The listed applicant is Royal Enterprises Manufacturing, Inc.. It received FDA 510(k) clearance on 1987-07-28 under 510(k) number K872518. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REM500 THREE WHEELED ELEC. CART.?

REM500 THREE WHEELED ELEC. CART. is a medical device that received FDA 510(k) clearance on 1987-07-28. The listed applicant is Royal Enterprises Manufacturing, Inc.. The 510(k) number is K872518.

When did REM500 THREE WHEELED ELEC. CART. receive FDA 510(k) clearance?

REM500 THREE WHEELED ELEC. CART. received FDA 510(k) clearance on 1987-07-28, under 510(k) number K872518.

Who is the listed applicant for REM500 THREE WHEELED ELEC. CART.?

The FDA 510(k) record lists Royal Enterprises Manufacturing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REM500 THREE WHEELED ELEC. CART.?

The FDA product code for REM500 THREE WHEELED ELEC. CART. is INI.

Related Clinical Trials

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Other records listing Royal Enterprises Manufacturing, Inc. as applicant

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.

K881766REM 250 THREE WHEELED ELECTRIC CART

Related Devices (Code: INI)

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

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