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FDA 510(k)

TRANS-ORAL DEPTH GAUGE

K-Number: K893415 · 1989-06-07

ApplicantRuggles Corp.
Decision Date1989-06-07
Product CodeLYQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRANS-ORAL DEPTH GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Ruggles Corp.. It received FDA 510(k) clearance on 1989-06-07 under 510(k) number K893415. The device is classified under product code LYQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANS-ORAL DEPTH GAUGE?

TRANS-ORAL DEPTH GAUGE is a medical device that received FDA 510(k) clearance on 1989-06-07. The listed applicant is Ruggles Corp.. The 510(k) number is K893415.

When did TRANS-ORAL DEPTH GAUGE receive FDA 510(k) clearance?

TRANS-ORAL DEPTH GAUGE received FDA 510(k) clearance on 1989-06-07, under 510(k) number K893415.

Who is the listed applicant for TRANS-ORAL DEPTH GAUGE?

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

What is the FDA product code for TRANS-ORAL DEPTH GAUGE?

The FDA product code for TRANS-ORAL DEPTH GAUGE is LYQ.

Related Clinical Trials

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Other records listing Ruggles Corp. 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.

K903485TITANIUM MESHK902818MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENTK902819LAMINECTOMY ROGEURK902850ZEPPELIN INSTRUMENTS

Related Devices (Code: LYQ)

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.

K883784TSRH ANTERIOR SPINAL SCREWS, STAPLES AND END PLATEWarsaw Orthopedic, Inc.K882871CASF DRILL GUIDE DG 170Terray Manufacturing, 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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