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FDA 510(k)

ENDO-SECURE

K-Number: K840844 · 1984-03-16

ApplicantExidyne, Inc.
Decision Date1984-03-16
Product CodeJAY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ENDO-SECURE is the device name listed in this FDA 510(k) record. The listed applicant is Exidyne, Inc.. It received FDA 510(k) clearance on 1984-03-16 under 510(k) number K840844. The device is classified under product code JAY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-SECURE?

ENDO-SECURE is a medical device that received FDA 510(k) clearance on 1984-03-16. The listed applicant is Exidyne, Inc.. The 510(k) number is K840844.

When did ENDO-SECURE receive FDA 510(k) clearance?

ENDO-SECURE received FDA 510(k) clearance on 1984-03-16, under 510(k) number K840844.

Who is the listed applicant for ENDO-SECURE?

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

What is the FDA product code for ENDO-SECURE?

The FDA product code for ENDO-SECURE is JAY.

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Related Devices (Code: JAY)

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.

K944988CUSTOM MEDICAL SUSPENSION STRAPCustom Medical Specialties, Inc.K873491BLOCK, BITE, INTUBATIONB&B Medical Technologies, Inc.K860583DALE HEAD BAND ANESTHESIA CIRCUIT TUBE HOLDER 1315Dale Medical Products, Inc.K850924JEE FRAME (VENTILATOR CIRCUIT SUPPORT)Vulcan Laboratories, Inc.K850309COMFIT PLUS ENDOTRACHEAL TUBE HOLDER & BITE BLOCKAckrad LaboratoriesK834265TRACH MATETempe Biomedical, 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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