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FDA 510(k)

EYE TRAY

K-Number: K912105 · 1991-08-29

ApplicantMedical Device Inspection Co., Inc.
Decision Date1991-08-29
Product CodeLRP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EYE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1991-08-29 under 510(k) number K912105. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EYE TRAY?

EYE TRAY is a medical device that received FDA 510(k) clearance on 1991-08-29. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K912105.

When did EYE TRAY receive FDA 510(k) clearance?

EYE TRAY received FDA 510(k) clearance on 1991-08-29, under 510(k) number K912105.

Who is the listed applicant for EYE TRAY?

The FDA 510(k) record lists Medical Device Inspection Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EYE TRAY?

The FDA product code for EYE TRAY is LRP.

Other records listing Medical Device Inspection Co., Inc. as applicant

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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 MedicalK940646ORTHOPEDIC TRAY PRODUCT LINECushinduK940444GENERAL SURGERY TRAYCush Medical Products

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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