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FDA 510(k)

SHAVE PREP TRAY

K-Number: K855132 · 1986-01-24

ApplicantDynarex Corp.
Decision Date1986-01-24
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SHAVE PREP TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Dynarex Corp.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K855132. 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 SHAVE PREP TRAY?

SHAVE PREP TRAY is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Dynarex Corp.. The 510(k) number is K855132.

When did SHAVE PREP TRAY receive FDA 510(k) clearance?

SHAVE PREP TRAY received FDA 510(k) clearance on 1986-01-24, under 510(k) number K855132.

Who is the listed applicant for SHAVE PREP TRAY?

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

What is the FDA product code for SHAVE PREP TRAY?

The FDA product code for SHAVE PREP TRAY is MDM.

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Other records listing Dynarex 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.

K052743DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921K052314DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGEK012816DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414K012957TOWEL DRAPE, MODELS 4409, 4410K012917DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-BK991695DYNAREX NON-WOVEN SPONGE

View all 19 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.

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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