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FDA 510(k)

CAMPION LASER FORCEPS

K-Number: K891348 · 1989-03-22

ApplicantSimpson/Basye, Inc.
Decision Date1989-03-22
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAMPION LASER FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Simpson/Basye, Inc.. It received FDA 510(k) clearance on 1989-03-22 under 510(k) number K891348. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPION LASER FORCEPS?

CAMPION LASER FORCEPS is a medical device that received FDA 510(k) clearance on 1989-03-22. The listed applicant is Simpson/Basye, Inc.. The 510(k) number is K891348.

When did CAMPION LASER FORCEPS receive FDA 510(k) clearance?

CAMPION LASER FORCEPS received FDA 510(k) clearance on 1989-03-22, under 510(k) number K891348.

Who is the listed applicant for CAMPION LASER FORCEPS?

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

What is the FDA product code for CAMPION LASER FORCEPS?

The FDA product code for CAMPION LASER FORCEPS is GEN.

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 Simpson/Basye, 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.

K926179SEDLACEK HANDLEK891352MARLOW ANAL SPECULUMK891351NEWPORT LATERAL VAGINAL RETRACTORK891350NEWPORT CERVICAL MANIPULATORK891349CAMPION CERVICAL HOOKK891347REID ENDOCERVICAL SPREADER

View all 12 devices →

Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900948GS-1002 GRASPING FORCEP, 5MM WITH RATCHETSolos Endoscopy, 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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