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FDA 510(k)

TROUTMAN CORNEAL PUNCH

K-Number: K771866 · 1977-11-09

ApplicantEdward Weck, Inc.
Decision Date1977-11-09
Product CodeHRH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TROUTMAN CORNEAL PUNCH 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 1977-11-09 under 510(k) number K771866. The device is classified under product code HRH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TROUTMAN CORNEAL PUNCH?

TROUTMAN CORNEAL PUNCH is a medical device that received FDA 510(k) clearance on 1977-11-09. The listed applicant is Edward Weck, Inc.. The 510(k) number is K771866.

When did TROUTMAN CORNEAL PUNCH receive FDA 510(k) clearance?

TROUTMAN CORNEAL PUNCH received FDA 510(k) clearance on 1977-11-09, under 510(k) number K771866.

Who is the listed applicant for TROUTMAN CORNEAL PUNCH?

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 TROUTMAN CORNEAL PUNCH?

The FDA product code for TROUTMAN CORNEAL PUNCH is HRH.

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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: HRH)

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.

K022843GAYHEART CORNEAL EXCISION DEVICEStephens InstrumentsK931792ARTHROSCOPEIntramed Laboratories, Inc.K873918HEAD & CHIN RESTSRichmond Products, Inc.K864520BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRONPrecision Instruments, Inc.K862524DEKNATEL (R) TREPHINEDeknatel, Inc.K861825CORNEAL TRANSPLANT TREPHINE DISPOSABLE BLADEStorz Instrument Co.

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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