FDA 510(k)

ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000

K-Number: K874243 · 1987-11-13

Decision Date1987-11-13

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000 is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1987-11-13 under 510(k) number K874243. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000?

ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000 is a medical device that received FDA 510(k) clearance on 1987-11-13. The listed applicant is Pilling Co.. The 510(k) number is K874243.

When did ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000 receive FDA 510(k) clearance?

ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000 received FDA 510(k) clearance on 1987-11-13, under 510(k) number K874243.

Who is the listed applicant for ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000?

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

What is the FDA product code for ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000?

The FDA product code for ABDOMINAL/VASCULAR RETRACTOR-SPLIT WISHBONE 163000 is GAD.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pilling Co. as applicant

K934427PILLING LAPAROSCOPIC INSTRUMENTATION K925370TRIANGULAR JAW MICROLARYNGEAL FORCEPS K925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTR K922971NO-SCALPEL VASCETOMY INSTRUMENTS K914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP K911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

View all 39 devices →

Related Devices (Code: GAD)

K152538JRP Wound SpreaderJ.R. Parker, LLC K151104OTELO LLSpineart K132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgical K050256APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTORApple Medical Corp.K043602QUADRANT RETRACTOR SYSTEMMedtronic Sofamor Danek

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.