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FDA 510(k)

SKIN SCRUB KITS

K-Number: K811855 · 1981-07-31

ApplicantOem Medical Div.
Decision Date1981-07-31
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKIN SCRUB KITS is the device name listed in this FDA 510(k) record. The listed applicant is Oem Medical Div.. It received FDA 510(k) clearance on 1981-07-31 under 510(k) number K811855. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIN SCRUB KITS?

SKIN SCRUB KITS is a medical device that received FDA 510(k) clearance on 1981-07-31. The listed applicant is Oem Medical Div.. The 510(k) number is K811855.

When did SKIN SCRUB KITS receive FDA 510(k) clearance?

SKIN SCRUB KITS received FDA 510(k) clearance on 1981-07-31, under 510(k) number K811855.

Who is the listed applicant for SKIN SCRUB KITS?

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

What is the FDA product code for SKIN SCRUB KITS?

The FDA product code for SKIN SCRUB KITS is KDD.

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.

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Other records listing Oem Medical Div. 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.

K924570OEM MULTI-VAC POWERED SUCTION PUMPK925893OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUITK922748GUEDEL AIRWAYK761297MOUTHPIECE SEAL

Related Devices (Code: KDD)

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.

K072814CONVENIENCE KIT FOR SINGLE-INCISION LAPAROSCOPIC SURGERY AND OTHER ADVANCED LAPAROSCOPIC PROCEDURESCovidienK011514INSTRUMENTS FOR ONE TIME USE - DISPOSABLEKencap , Ltd.K971317NATIONAL MEDICAL HEALTHCARE CUSTOM ORTHOPEDIC KITS AND TRAYSNational Healthcare Mfg. Corp.K960456DENVER PARACENTESIS NEEDLE(60-1200) DENVER PARACENTESIS NEEDLE WITH DRAINAGE LINE(60-1100) DENVER PARACENTESIS TRAYDenver Biomaterials, Inc.K936255CUSTOM CV PACKAssociated MedicalK932219SUTURE SET OR LACERATION TRAYS (PACKS)Associated Medical Products Co.

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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