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FDA 510(k)

ANESTHESIOMETER

K-Number: K851557 · 1985-05-30

ApplicantLuneau SA
Decision Date1985-05-30
Product CodeHJC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ANESTHESIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Luneau SA. It received FDA 510(k) clearance on 1985-05-30 under 510(k) number K851557. The device is classified under product code HJC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIOMETER?

ANESTHESIOMETER is a medical device that received FDA 510(k) clearance on 1985-05-30. The listed applicant is Luneau SA. The 510(k) number is K851557.

When did ANESTHESIOMETER receive FDA 510(k) clearance?

ANESTHESIOMETER received FDA 510(k) clearance on 1985-05-30, under 510(k) number K851557.

Who is the listed applicant for ANESTHESIOMETER?

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

What is the FDA product code for ANESTHESIOMETER?

The FDA product code for ANESTHESIOMETER is HJC.

Related Clinical Trials

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.

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Other records listing Luneau SA 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.

K023838LUNEAU STERILE TONOMETER SEPARATION PRISMSK022413LUNEAU 3 MIRROR LENS

Related Devices (Code: HJC)

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.

K920271WEINSTEIN CORNEAL MIRCOAESTHESIOMETERConnecticut Bioinstruments, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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