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FDA 510(k)

ANESTHESIA KIT

K-Number: K760759 · 1976-12-09

ApplicantSherwood Medical Industries
Decision Date1976-12-09
Product CodeCCT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K760759. The device is classified under product code CCT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA KIT?

ANESTHESIA KIT is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760759.

When did ANESTHESIA KIT receive FDA 510(k) clearance?

ANESTHESIA KIT received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760759.

Who is the listed applicant for ANESTHESIA KIT?

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

What is the FDA product code for ANESTHESIA KIT?

The FDA product code for ANESTHESIA KIT is CCT.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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Related Devices (Code: CCT)

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.

K240114UltraEzAir® (UEA1A)Dualams, Inc., Dba AirkorK172956Medicant Mucosal AtomizerMedica Holdings, LLCK153470MADgic Laryngo-Tracheal Mucosal Atomization DeviceTeleflex MedicalK093584EZ-MISTERN.M. Beale Co., Inc.K070596TOPICAL APPLICATORSharn, Inc.K002255LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE (MADGIC)Wolfe Tory Medical, 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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