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FDA 510(k)

STERILE INSTRUMENT TRAYS/BASIN SETS

K-Number: K924468 · 1993-07-09

Decision Date1993-07-09
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE INSTRUMENT TRAYS/BASIN SETS is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1993-07-09 under 510(k) number K924468. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE INSTRUMENT TRAYS/BASIN SETS?

STERILE INSTRUMENT TRAYS/BASIN SETS is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K924468.

When did STERILE INSTRUMENT TRAYS/BASIN SETS receive FDA 510(k) clearance?

STERILE INSTRUMENT TRAYS/BASIN SETS received FDA 510(k) clearance on 1993-07-09, under 510(k) number K924468.

Who is the listed applicant for STERILE INSTRUMENT TRAYS/BASIN SETS?

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

What is the FDA product code for STERILE INSTRUMENT TRAYS/BASIN SETS?

The FDA product code for STERILE INSTRUMENT TRAYS/BASIN SETS is LRO.

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.

Other records listing Baxter Healthcare 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.

View all 504 devices →

Related Devices (Code: LRO)

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.

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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