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FDA 510(k)

PEOPLE MOVER

K-Number: K822992 · 1982-10-27

ApplicantConvaid Products, Inc.
Decision Date1982-10-27
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PEOPLE MOVER is the device name listed in this FDA 510(k) record. The listed applicant is Convaid Products, Inc.. It received FDA 510(k) clearance on 1982-10-27 under 510(k) number K822992. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEOPLE MOVER?

PEOPLE MOVER is a medical device that received FDA 510(k) clearance on 1982-10-27. The listed applicant is Convaid Products, Inc.. The 510(k) number is K822992.

When did PEOPLE MOVER receive FDA 510(k) clearance?

PEOPLE MOVER received FDA 510(k) clearance on 1982-10-27, under 510(k) number K822992.

Who is the listed applicant for PEOPLE MOVER?

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

What is the FDA product code for PEOPLE MOVER?

The FDA product code for PEOPLE MOVER is INM.

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Other records listing Convaid Products, 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.

K120501CHAMP CHAMP TRANSITK032402RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,K840250CARRIERK833195UMBRELLA WALKERK810676CONVAID CRUISER CP4MK781947STROLLER, THERAPY

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Related Devices (Code: INM)

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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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