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FDA 510(k)

KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)

K-Number: K853727 · 1986-02-07

ApplicantRyder Intl. Corp.
Decision Date1986-02-07
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE) is the device name listed in this FDA 510(k) record. The listed applicant is Ryder Intl. Corp.. It received FDA 510(k) clearance on 1986-02-07 under 510(k) number K853727. 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 CONTACT LENS STORAGE CASE(POLYSULFONE)?

KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE) is a medical device that received FDA 510(k) clearance on 1986-02-07. The listed applicant is Ryder Intl. Corp.. The 510(k) number is K853727.

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

KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE) received FDA 510(k) clearance on 1986-02-07, under 510(k) number K853727.

Who is the listed applicant for KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)?

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

What is the FDA product code for KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE)?

The FDA product code for KESTREL CONTACT LENS STORAGE CASE(POLYSULFONE) is LRX.

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Other records listing Ryder Intl. Corp. 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.

K962611BARD EAGLE INFLATION DEVICEK962151RYDER LACRIMAL INTUBATIONSETK953522USCI IDEAL PTCA KITK920064OPTI-LENS CONTACT LENS CASEK915082OPTI-LENS(TM) CONTACT LENS CASEK881981ASSIST(TM) ASEPTIC SYRINGE IRRIGATION SYSTEM

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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

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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