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FDA 510(k)

GEN. PURPOSE INSTRUMENT TRAYS &

K-Number: K833058 · 1984-01-31

ApplicantInter-Med Corp.
Decision Date1984-01-31
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GEN. PURPOSE INSTRUMENT TRAYS & is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med Corp.. It received FDA 510(k) clearance on 1984-01-31 under 510(k) number K833058. 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 GEN. PURPOSE INSTRUMENT TRAYS &?

GEN. PURPOSE INSTRUMENT TRAYS & is a medical device that received FDA 510(k) clearance on 1984-01-31. The listed applicant is Inter-Med Corp.. The 510(k) number is K833058.

When did GEN. PURPOSE INSTRUMENT TRAYS & receive FDA 510(k) clearance?

GEN. PURPOSE INSTRUMENT TRAYS & received FDA 510(k) clearance on 1984-01-31, under 510(k) number K833058.

Who is the listed applicant for GEN. PURPOSE INSTRUMENT TRAYS &?

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

What is the FDA product code for GEN. PURPOSE INSTRUMENT TRAYS &?

The FDA product code for GEN. PURPOSE INSTRUMENT TRAYS & is FSM.

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Other records listing Inter-Med 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.

K871291AM CATH ESWL STENTK864669AM CATH ESWL STENTK851922URETERAL STONE DISLODGER

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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