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FDA 510(k)

SURGICAL LASER ACCESSORIES (SLA) CASE

K-Number: K862629 · 1986-07-17

ApplicantSimpson/Basye, Inc.
Decision Date1986-07-17
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL LASER ACCESSORIES (SLA) CASE 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 1986-07-17 under 510(k) number K862629. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL LASER ACCESSORIES (SLA) CASE?

SURGICAL LASER ACCESSORIES (SLA) CASE is a medical device that received FDA 510(k) clearance on 1986-07-17. The listed applicant is Simpson/Basye, Inc.. The 510(k) number is K862629.

When did SURGICAL LASER ACCESSORIES (SLA) CASE receive FDA 510(k) clearance?

SURGICAL LASER ACCESSORIES (SLA) CASE received FDA 510(k) clearance on 1986-07-17, under 510(k) number K862629.

Who is the listed applicant for SURGICAL LASER ACCESSORIES (SLA) CASE?

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 SURGICAL LASER ACCESSORIES (SLA) CASE?

The FDA product code for SURGICAL LASER ACCESSORIES (SLA) CASE is FSM.

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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 RETRACTORK891347REID ENDOCERVICAL SPREADERK891349CAMPION CERVICAL HOOKK891350NEWPORT CERVICAL MANIPULATOR

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Related Devices (Code: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection 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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