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FDA 510(k)

SLIP-PRUF-CLINGER

K-Number: K913049 · 1991-09-11

ApplicantMacbrud Corp. Medical Div.
Decision Date1991-09-11
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SLIP-PRUF-CLINGER is the device name listed in this FDA 510(k) record. The listed applicant is Macbrud Corp. Medical Div.. It received FDA 510(k) clearance on 1991-09-11 under 510(k) number K913049. 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 SLIP-PRUF-CLINGER?

SLIP-PRUF-CLINGER is a medical device that received FDA 510(k) clearance on 1991-09-11. The listed applicant is Macbrud Corp. Medical Div.. The 510(k) number is K913049.

When did SLIP-PRUF-CLINGER receive FDA 510(k) clearance?

SLIP-PRUF-CLINGER received FDA 510(k) clearance on 1991-09-11, under 510(k) number K913049.

Who is the listed applicant for SLIP-PRUF-CLINGER?

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

What is the FDA product code for SLIP-PRUF-CLINGER?

The FDA product code for SLIP-PRUF-CLINGER 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Macbrud Corp. 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.

K911873X-MARXK900282NEEDLE-SHIELDK891090SPECBOARD

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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