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FDA 510(k)

HOSPITAL KIT DK 117

K-Number: K922130 · 1993-05-24

ApplicantSavoy Medical Supply Co., Inc.
Decision Date1993-05-24
Product CodeMDM
Advisory CommitteeSU
DecisionUnknown

Device Summary

HOSPITAL KIT DK 117 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 1993-05-24 under 510(k) number K922130. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the HOSPITAL KIT DK 117?

HOSPITAL KIT DK 117 is a medical device that received FDA 510(k) clearance on 1993-05-24. The listed applicant is Savoy Medical Supply Co., Inc.. The 510(k) number is K922130.

When did HOSPITAL KIT DK 117 receive FDA 510(k) clearance?

HOSPITAL KIT DK 117 received FDA 510(k) clearance on 1993-05-24, under 510(k) number K922130.

Who is the listed applicant for HOSPITAL KIT DK 117?

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 HOSPITAL KIT DK 117?

The FDA product code for HOSPITAL KIT DK 117 is MDM.

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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 105K922127HOSPITAL KIT GP 103K923281SV 100200 - SINGLE USE ONLY - STERILE HOSPITAL KITK922128HOSPITAL KIT EP 104K922126HOSPITAL KIT ENT 1125K923283SUP 5415 SINGLE USE ONLY STERILE HOSPITAL KIT

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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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK013040LIGHT SABER INTRODUCER NEEDLEMinrad, Inc.

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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