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FDA 510(k)

BEAVER CATARACT CYROXTRACTOR

K-Number: K781338 · 1979-02-12

ApplicantEdward Weck, Inc.
Decision Date1979-02-12
Product CodeHPS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BEAVER CATARACT CYROXTRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1979-02-12 under 510(k) number K781338. The device is classified under product code HPS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAVER CATARACT CYROXTRACTOR?

BEAVER CATARACT CYROXTRACTOR is a medical device that received FDA 510(k) clearance on 1979-02-12. The listed applicant is Edward Weck, Inc.. The 510(k) number is K781338.

When did BEAVER CATARACT CYROXTRACTOR receive FDA 510(k) clearance?

BEAVER CATARACT CYROXTRACTOR received FDA 510(k) clearance on 1979-02-12, under 510(k) number K781338.

Who is the listed applicant for BEAVER CATARACT CYROXTRACTOR?

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

What is the FDA product code for BEAVER CATARACT CYROXTRACTOR?

The FDA product code for BEAVER CATARACT CYROXTRACTOR is HPS.

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Other records listing Edward Weck, 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.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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Related Devices (Code: HPS)

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.

K202038CryoTreQVitreQ BVK940373OPHTHALMIC CRYO UNITDutch Ophthalmic USA, Inc.K923629OPHTHALMIC TRICHIASIS PROBEMira, Inc.K903303SPEMBLY MEDICAL 242 CRYOUNIT/SERIES 242 CRYOPROBESSpembly Medical , Ltd.K874555KEELER ACU 22XT OPHTHALMIC CRYO UNITKeeler Instruments, Inc.K873388KEELER CTU CRYO SYSTEMKeeler Instruments, 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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