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FDA 510(k)

SUTURE REMOVAL TRAY

K-Number: K902828 · 1990-08-08

ApplicantOrion Life Systems, Inc.
Decision Date1990-08-08
Product CodeLRW
Advisory CommitteeSU
DecisionUnknown

Device Summary

SUTURE REMOVAL TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Orion Life Systems, Inc.. It received FDA 510(k) clearance on 1990-08-08 under 510(k) number K902828. The device is classified under product code LRW. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SUTURE REMOVAL TRAY?

SUTURE REMOVAL TRAY is a medical device that received FDA 510(k) clearance on 1990-08-08. The listed applicant is Orion Life Systems, Inc.. The 510(k) number is K902828.

When did SUTURE REMOVAL TRAY receive FDA 510(k) clearance?

SUTURE REMOVAL TRAY received FDA 510(k) clearance on 1990-08-08, under 510(k) number K902828.

Who is the listed applicant for SUTURE REMOVAL TRAY?

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

What is the FDA product code for SUTURE REMOVAL TRAY?

The FDA product code for SUTURE REMOVAL TRAY is LRW.

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Related Devices (Code: LRW)

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.

K911158MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MMNorthgate Technologies, Inc.K900957GS-2100 HOOK SUTURE SCISSOR, 5MMSolos Endoscopy, Inc.K900950GS-2000 MICRO SCISSOR, CURVED LEFT, 5MMSolos Endoscopy, Inc.K892823PLASTER CUTTING SCISSORSThe South India Surgical Co. Pvt. , Ltd.K891889OLIVECORONA SCISSORSZinnanti Surgical Instruments, Inc.K891886SCISSORS, VARIOUS TYPESZinnanti Surgical Instruments, 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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