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FDA 510(k)

OMNIPATCH

K-Number: K900941 · 1990-05-21

ApplicantEye Garter Company, Inc.
Decision Date1990-05-21
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OMNIPATCH is the device name listed in this FDA 510(k) record. The listed applicant is Eye Garter Company, Inc.. It received FDA 510(k) clearance on 1990-05-21 under 510(k) number K900941. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNIPATCH?

OMNIPATCH is a medical device that received FDA 510(k) clearance on 1990-05-21. The listed applicant is Eye Garter Company, Inc.. The 510(k) number is K900941.

When did OMNIPATCH receive FDA 510(k) clearance?

OMNIPATCH received FDA 510(k) clearance on 1990-05-21, under 510(k) number K900941.

Who is the listed applicant for OMNIPATCH?

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

What is the FDA product code for OMNIPATCH?

The FDA product code for OMNIPATCH is HOY.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Eye Garter Company, 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.

K896171EYE PATCHK896172STRAPPED EYE SHIELDK880489CLEAR EYE GARTER SHIELDK880490BLUE PLASTIC EYE SHIELDK880675EASY SHIELD ADHESIVE BANDAGE

Related Devices (Code: HOY)

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.

K050856LCG (LIQUIDE CRYSTAL GLASSES) SYSTEMOphthocare , Ltd.K971465NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYSNational Healthcare Mfg. Corp.K944700ARCTIC PREMIER SERIESSungold Eyewear, Inc.K944857GOGGLE SAFEGUARDSellstrom Mfg. Co.K945351SHIELD, EYE, OPHTHALMICTaiwan Eva Industrial Co., Inc.K945346MAKROLON 2405 GOGGLES (LIGHT AND DARK)Universal Massage & Tanning, 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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