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FDA 510(k)

KESTREL LENS CASE 731H-893S/P-1700-2611

K-Number: K900053 · 1990-01-30

ApplicantKestrel
Decision Date1990-01-30
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KESTREL LENS CASE 731H-893S/P-1700-2611 is the device name listed in this FDA 510(k) record. The listed applicant is Kestrel. It received FDA 510(k) clearance on 1990-01-30 under 510(k) number K900053. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KESTREL LENS CASE 731H-893S/P-1700-2611?

KESTREL LENS CASE 731H-893S/P-1700-2611 is a medical device that received FDA 510(k) clearance on 1990-01-30. The listed applicant is Kestrel. The 510(k) number is K900053.

When did KESTREL LENS CASE 731H-893S/P-1700-2611 receive FDA 510(k) clearance?

KESTREL LENS CASE 731H-893S/P-1700-2611 received FDA 510(k) clearance on 1990-01-30, under 510(k) number K900053.

Who is the listed applicant for KESTREL LENS CASE 731H-893S/P-1700-2611?

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

What is the FDA product code for KESTREL LENS CASE 731H-893S/P-1700-2611?

The FDA product code for KESTREL LENS CASE 731H-893S/P-1700-2611 is LRX.

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Other records listing Kestrel 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.

K901748KESTREL LENS CASE (208-12NT POLYSTYRENE)K900054KESTREL LENS CASE 1543-893S/P-1700-2611

Related Devices (Code: LRX)

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.

K252175LANDR Contact LENS CaseFourth Axis, LLCK250495MINI VP1 (PL67_F); MINI VP1 (PL61_F)Avizor S.A.K240095CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)Shanghai Care US Medical Product Co., Ltd.K231123Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case - classic flat pack (CL-02); Phoenix Contact Lens Case - sunglass shape flat pack (CL-03)Phoenix Innovative Healthcare Manufacturers Pvt. , Ltd.K173538Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscAlcon Laboratories, Inc.K172925Contact Lens Case, Model: A-1, B-1P L Overseas Limited

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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