FDA 510(k)

STERILE LACERATION TRAY

K-Number: K890071 · 1989-01-24

Decision Date1989-01-24

Product CodeLRP

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STERILE LACERATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Mumtaz I. Malik. It received FDA 510(k) clearance on 1989-01-24 under 510(k) number K890071. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE LACERATION TRAY?

STERILE LACERATION TRAY is a medical device that received FDA 510(k) clearance on 1989-01-24. The listed applicant is Mumtaz I. Malik. The 510(k) number is K890071.

When did STERILE LACERATION TRAY receive FDA 510(k) clearance?

STERILE LACERATION TRAY received FDA 510(k) clearance on 1989-01-24, under 510(k) number K890071.

Who is the listed applicant for STERILE LACERATION TRAY?

The FDA 510(k) record lists Mumtaz I. Malik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE LACERATION TRAY?

The FDA product code for STERILE LACERATION TRAY is LRP.

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Other records listing Mumtaz I. Malik as applicant

K901289RONGEUR, ORTHOPEDIC SURGICAL INSTRUMENTS K901521OSTEOTOMES OF VARIOUS TYPES K901420VOLKMAN BONE CURRETTE 5, 5-3/4, 6-3/4, 8 K901511CHISEL, BONE, SURGICAL K8939024 X 4 STERILE GAUZE SPONGE TRAY K884195GENERAL SURGICAL INSTRUMENTS (VARIOUS TYPES)

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Related Devices (Code: LRP)

K963723LACERATION TRAYGrand Medical Products K951811OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACKOsteotech, Inc.K940239EYE TRAYCush Medical Products K935621CUSTOM ENT PACKSAssociated Medical K940646ORTHOPEDIC TRAY PRODUCT LINECushindu K940444GENERAL SURGERY TRAYCush Medical Products

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.