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FDA 510(k)

CARRIER

K-Number: K840250 · 1984-02-09

ApplicantConvaid Products, Inc.
Decision Date1984-02-09
Product CodeLBE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CARRIER 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 1984-02-09 under 510(k) number K840250. The device is classified under product code LBE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARRIER?

CARRIER is a medical device that received FDA 510(k) clearance on 1984-02-09. The listed applicant is Convaid Products, Inc.. The 510(k) number is K840250.

When did CARRIER receive FDA 510(k) clearance?

CARRIER received FDA 510(k) clearance on 1984-02-09, under 510(k) number K840250.

Who is the listed applicant for CARRIER?

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 CARRIER?

The FDA product code for CARRIER is LBE.

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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Related PubMed Literature

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.

PMID: 29111623Medical Devices; Exemption From Premarket Notification; Class II Devices; Autosomal Recessive Carrier Screening Gene Mutation Detection System. Final order.Federal register ()

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,K833195UMBRELLA WALKERK822992PEOPLE MOVERK810676CONVAID CRUISER CP4MK781947STROLLER, THERAPY

View all 7 devices →

Related Devices (Code: LBE)

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.

K223533Little Wave Arc; Little Wave FlipKi Mobility, LLCK130644PEDIATRIC FOLDING WHEELCHAIRColumbia Medical Mfg, LLCK863450SULKY SPECIALAsc Corp.K862888PERAMBULATOR (STROLLER)Mednet, Inc.K820591MECHANICAL CHAIRKaye Products, Inc.K810676CONVAID CRUISER CP4MConvaid Products, Inc.

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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