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FDA 510(k)

GLENROE BAND SEATING CONTOURING INSTRUMENT

K-Number: K924993 · 1992-11-25

ApplicantGlenroe Technologies
Decision Date1992-11-25
Product CodeECS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GLENROE BAND SEATING CONTOURING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Glenroe Technologies. It received FDA 510(k) clearance on 1992-11-25 under 510(k) number K924993. The device is classified under product code ECS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLENROE BAND SEATING CONTOURING INSTRUMENT?

GLENROE BAND SEATING CONTOURING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1992-11-25. The listed applicant is Glenroe Technologies. The 510(k) number is K924993.

When did GLENROE BAND SEATING CONTOURING INSTRUMENT receive FDA 510(k) clearance?

GLENROE BAND SEATING CONTOURING INSTRUMENT received FDA 510(k) clearance on 1992-11-25, under 510(k) number K924993.

Who is the listed applicant for GLENROE BAND SEATING CONTOURING INSTRUMENT?

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

What is the FDA product code for GLENROE BAND SEATING CONTOURING INSTRUMENT?

The FDA product code for GLENROE BAND SEATING CONTOURING INSTRUMENT is ECS.

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Other records listing Glenroe Technologies 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.

K980053GLENROE CHAINK945535GLENROE ORTHO-SILK924351GLENROE ELASTIBITE STIMULATORK932920GLENROE PLASTIC BRACKETK924140TUFF TIESK924139GLENROE ORTHO SEPS

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Related Devices (Code: ECS)

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.

K935155MERSHON BAND PUSHERDentauraum, 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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