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FDA 510(k)

LIGHTCAST II CARBIDE BLADE

K-Number: K760605 · 1976-10-05

ApplicantMerck, Sharp & Dohme
Decision Date1976-10-05
Product CodeGES
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHTCAST II CARBIDE BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Merck, Sharp & Dohme. It received FDA 510(k) clearance on 1976-10-05 under 510(k) number K760605. The device is classified under product code GES. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHTCAST II CARBIDE BLADE?

LIGHTCAST II CARBIDE BLADE is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Merck, Sharp & Dohme. The 510(k) number is K760605.

When did LIGHTCAST II CARBIDE BLADE receive FDA 510(k) clearance?

LIGHTCAST II CARBIDE BLADE received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760605.

Who is the listed applicant for LIGHTCAST II CARBIDE BLADE?

The FDA 510(k) record lists Merck, Sharp & Dohme as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHTCAST II CARBIDE BLADE?

The FDA product code for LIGHTCAST II CARBIDE BLADE is GES.

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Other records listing Merck, Sharp & Dohme 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.

K880574MODIFIED IMIPENEM SUSCEPTIBILITY POWDERK864442NORFLOXACIN SUSCEPTIBILITY POWDERK855071IMIPENEM SUSCEPTIBILITY POWDER

Related Devices (Code: GES)

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.

K032242PERSONNA PLUS SAFETY SCALPEL SYSTEMOmi Manufacturing Pty., Ltd.K932998EASY-ONDevon Industries, Inc.K923170LOS ALAMOS RETRACTABLE KNIFEInnovative Surgical Technology, Inc.K915119SCALPEL BLADE REMOVER (BLADEGARD)Intergrated Visual, Inc.K911913PRECISION GLIDE - ENHANCED SURGICAL BLADEBd Becton Dickinson Vacutainer Systems PreanalyticK900266STERILE CARBON STEEL SURGICAL BLADERahn Laboratories

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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