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FDA 510(k)

SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT

K-Number: K923283 · 1993-01-04

ApplicantSavoy Medical Supply Co., Inc.
Decision Date1993-01-04
Product CodeKKX
Advisory CommitteeSU
DecisionUnknown

Device Summary

SUP 5415 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 1993-01-04 under 510(k) number K923283. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT?

SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT is a medical device that received FDA 510(k) clearance on 1993-01-04. The listed applicant is Savoy Medical Supply Co., Inc.. The 510(k) number is K923283.

When did SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT receive FDA 510(k) clearance?

SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT received FDA 510(k) clearance on 1993-01-04, under 510(k) number K923283.

Who is the listed applicant for SUP 5415 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 SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT?

The FDA product code for SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT is KKX.

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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.

K922133HOSPITAL KIT SV 105K922130HOSPITAL KIT DK 117K922127HOSPITAL KIT GP 103K923281SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KITK922128HOSPITAL KIT EP 104K922126HOSPITAL KIT ENT 1125

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Related Devices (Code: KKX)

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.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

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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