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FDA 510(k)

RAYLOR(TM) DEPTH GAUGE

K-Number: K864426 · 1986-11-26

ApplicantCedar Surgical, Inc.
Decision Date1986-11-26
Product CodeHTJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RAYLOR(TM) DEPTH GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Cedar Surgical, Inc.. It received FDA 510(k) clearance on 1986-11-26 under 510(k) number K864426. The device is classified under product code HTJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAYLOR(TM) DEPTH GAUGE?

RAYLOR(TM) DEPTH GAUGE is a medical device that received FDA 510(k) clearance on 1986-11-26. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K864426.

When did RAYLOR(TM) DEPTH GAUGE receive FDA 510(k) clearance?

RAYLOR(TM) DEPTH GAUGE received FDA 510(k) clearance on 1986-11-26, under 510(k) number K864426.

Who is the listed applicant for RAYLOR(TM) DEPTH GAUGE?

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

What is the FDA product code for RAYLOR(TM) DEPTH GAUGE?

The FDA product code for RAYLOR(TM) DEPTH GAUGE is HTJ.

Related Clinical Trials

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Other records listing Cedar Surgical, 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.

K873692RAYLOR(TM) DRILL STOPK872281RAYLOR FUSION FUNNELK873690CEDAR(TM) PELVIC CUSHIONK873691CEDAR(TM) RETRACTOR RINGK864425RAYLOR(TM) DISSECTING HOOKK864424RAYLOR(TM) PROTECTIVE RETRACTOR

View all 17 devices →

Related Devices (Code: HTJ)

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.

K940480ACUFEX SUB-ACROMIAL SPACE MEASURING DEVICEAcufex Microsurgical, Inc.K925335ACUFEX INTRA ARTICULAR MEASURING DEVICEAcufex Microsurgical, Inc.K873191ACROMED INTERBODY DEPTH GAUGESBuckman Co., 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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