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FDA 510(k)

ORTHOPEDIC TRAY PRODUCT LINE

K-Number: K940646 · 1994-03-11

ApplicantCushindu
Decision Date1994-03-11
Product CodeLRP
Advisory CommitteeSU
DecisionUnknown

Device Summary

ORTHOPEDIC TRAY PRODUCT LINE is the device name listed in this FDA 510(k) record. The listed applicant is Cushindu. It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K940646. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ORTHOPEDIC TRAY PRODUCT LINE?

ORTHOPEDIC TRAY PRODUCT LINE is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Cushindu. The 510(k) number is K940646.

When did ORTHOPEDIC TRAY PRODUCT LINE receive FDA 510(k) clearance?

ORTHOPEDIC TRAY PRODUCT LINE received FDA 510(k) clearance on 1994-03-11, under 510(k) number K940646.

Who is the listed applicant for ORTHOPEDIC TRAY PRODUCT LINE?

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

What is the FDA product code for ORTHOPEDIC TRAY PRODUCT LINE?

The FDA product code for ORTHOPEDIC TRAY PRODUCT LINE is LRP.

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Related Devices (Code: LRP)

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.

K963723LACERATION TRAYGrand Medical ProductsK951811OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACKOsteotech, Inc.K940239EYE TRAYCush Medical ProductsK935621CUSTOM ENT PACKSAssociated MedicalK940444GENERAL SURGERY TRAYCush Medical ProductsK922126HOSPITAL KIT ENT 1125Savoy Medical Supply Co., Inc.

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.

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