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FDA 510(k)

ACCESSORY TO EYEDROP GUIDE

K-Number: K884974 · 1989-03-24

ApplicantSuredrop, Inc.
Decision Date1989-03-24
Product CodeJYJ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ACCESSORY TO EYEDROP GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Suredrop, Inc.. It received FDA 510(k) clearance on 1989-03-24 under 510(k) number K884974. The device is classified under product code JYJ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCESSORY TO EYEDROP GUIDE?

ACCESSORY TO EYEDROP GUIDE is a medical device that received FDA 510(k) clearance on 1989-03-24. The listed applicant is Suredrop, Inc.. The 510(k) number is K884974.

When did ACCESSORY TO EYEDROP GUIDE receive FDA 510(k) clearance?

ACCESSORY TO EYEDROP GUIDE received FDA 510(k) clearance on 1989-03-24, under 510(k) number K884974.

Who is the listed applicant for ACCESSORY TO EYEDROP GUIDE?

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

What is the FDA product code for ACCESSORY TO EYEDROP GUIDE?

The FDA product code for ACCESSORY TO EYEDROP GUIDE is JYJ.

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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Other records listing Suredrop, 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.

K874569SUREDROP EYEDROP GUIDE

Related Devices (Code: JYJ)

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.

K904469EYEOPENERKc Medical IndustriesK874569SUREDROP EYEDROP GUIDESuredrop, Inc.K833606IMPLANT MEASURING GAUGEMicrotek Medical, Inc.K801938RHINOMETERAztec Medical 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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