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FDA 510(k)

KESTREL CONTACT LENS CASE

K-Number: K871714 · 1987-05-26

ApplicantApplied Laboratories, Inc.
Decision Date1987-05-26
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KESTREL CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Applied Laboratories, Inc.. It received FDA 510(k) clearance on 1987-05-26 under 510(k) number K871714. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KESTREL CONTACT LENS CASE?

KESTREL CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1987-05-26. The listed applicant is Applied Laboratories, Inc.. The 510(k) number is K871714.

When did KESTREL CONTACT LENS CASE receive FDA 510(k) clearance?

KESTREL CONTACT LENS CASE received FDA 510(k) clearance on 1987-05-26, under 510(k) number K871714.

Who is the listed applicant for KESTREL CONTACT LENS CASE?

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

What is the FDA product code for KESTREL CONTACT LENS CASE?

The FDA product code for KESTREL CONTACT LENS CASE is LPN.

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Other records listing Applied Laboratories, 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.

K873824RED #467, #457, BLUE #437, GREEN #447 MINDEL S1000K873821GE NORYL 731-80089SK873820MOBAY (BAYER) MAKROLON 2658 1112K873823MOBAY (BAYER) MAKROLON 2658 3291K873822MOBAY (BAYER) MERLON M-40 (H)F 1112K873825GE LEXAN 144R 112

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Related Devices (Code: LPN)

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.

K253795MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting SolutionMenicon Co, Ltd.K222541Bausch + Lomb Preservative Free Lubricating and Rewetting DropsBausch & Lomb, IncorporatedK221263Aqua Naina Plus Sterile Saline SolutionChemtex USA, Inc.K202932ABT12 multi-purpose solutionBausch & Lomb, IncorporatedK210051OTE MPS 045 Multi-purpose Lens Care SolutionOte North America, LLCK193441Aqua Naina Sterile Saline SolutionChemtex USA, 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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