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FDA 510(k)

CONCEPT SWITCHING STICK

K-Number: K873009 · 1987-08-17

ApplicantConcept, Inc.
Decision Date1987-08-17
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONCEPT SWITCHING STICK is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1987-08-17 under 510(k) number K873009. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONCEPT SWITCHING STICK?

CONCEPT SWITCHING STICK is a medical device that received FDA 510(k) clearance on 1987-08-17. The listed applicant is Concept, Inc.. The 510(k) number is K873009.

When did CONCEPT SWITCHING STICK receive FDA 510(k) clearance?

CONCEPT SWITCHING STICK received FDA 510(k) clearance on 1987-08-17, under 510(k) number K873009.

Who is the listed applicant for CONCEPT SWITCHING STICK?

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

What is the FDA product code for CONCEPT SWITCHING STICK?

The FDA product code for CONCEPT SWITCHING STICK is KGZ.

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Other records listing Concept, 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.

K912640CONCEPT ENDOSTEAL FIXATION DEVICEK912957CONCEPT MICROMILLK896648CONCEPT UNICOMPARTMENTAL KNEE SYSTEMK894929STAPLE FIXATION SYSTEMK892376INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)K891109PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE

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Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.

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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