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FDA 510(k)

SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT

K-Number: K923281 · 1993-03-26

Decision Date1993-03-26
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Savoy Medical Supply Co., Inc.. It received FDA 510(k) clearance on 1993-03-26 under 510(k) number K923281. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT?

SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT is a medical device that received FDA 510(k) clearance on 1993-03-26. The listed applicant is Savoy Medical Supply Co., Inc.. The 510(k) number is K923281.

When did SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT receive FDA 510(k) clearance?

SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT received FDA 510(k) clearance on 1993-03-26, under 510(k) number K923281.

Who is the listed applicant for SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT?

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

What is the FDA product code for SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT?

The FDA product code for SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KIT is MDM.

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 Savoy Medical Supply Co., Inc. 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 7 devices →

Related Devices (Code: MDM)

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

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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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