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FDA 510(k)

FIRST RESPONSE EMERG. EYE INJURIES

K-Number: K841900 · 1984-07-23

Decision Date1984-07-23
Product CodeLRR
DecisionSubstantially Equivalent

Device Summary

FIRST RESPONSE EMERG. EYE INJURIES is the device name listed in this FDA 510(k) record. The listed applicant is Reed Products, Inc.. It received FDA 510(k) clearance on 1984-07-23 under 510(k) number K841900. The device is classified under product code LRR. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST RESPONSE EMERG. EYE INJURIES?

FIRST RESPONSE EMERG. EYE INJURIES is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is Reed Products, Inc.. The 510(k) number is K841900.

When did FIRST RESPONSE EMERG. EYE INJURIES receive FDA 510(k) clearance?

FIRST RESPONSE EMERG. EYE INJURIES received FDA 510(k) clearance on 1984-07-23, under 510(k) number K841900.

Who is the listed applicant for FIRST RESPONSE EMERG. EYE INJURIES?

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

What is the FDA product code for FIRST RESPONSE EMERG. EYE INJURIES?

The FDA product code for FIRST RESPONSE EMERG. EYE INJURIES is LRR.

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.

Other records listing Reed Products, 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.

Related Devices (Code: LRR)

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.

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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