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FDA 510(k)

STERILE DISPOSABLE WET SKIN SCRUB TRAY

K-Number: K914174 · 1992-02-24

ApplicantMedical Device Inspection Co., Inc.
Decision Date1992-02-24
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

STERILE DISPOSABLE WET SKIN SCRUB TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1992-02-24 under 510(k) number K914174. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the STERILE DISPOSABLE WET SKIN SCRUB TRAY?

STERILE DISPOSABLE WET SKIN SCRUB TRAY is a medical device that received FDA 510(k) clearance on 1992-02-24. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K914174.

When did STERILE DISPOSABLE WET SKIN SCRUB TRAY receive FDA 510(k) clearance?

STERILE DISPOSABLE WET SKIN SCRUB TRAY received FDA 510(k) clearance on 1992-02-24, under 510(k) number K914174.

Who is the listed applicant for STERILE DISPOSABLE WET SKIN SCRUB TRAY?

The FDA 510(k) record lists Medical Device Inspection Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE DISPOSABLE WET SKIN SCRUB TRAY?

The FDA product code for STERILE DISPOSABLE WET SKIN SCRUB TRAY is LRO.

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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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