Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RANEY CLIP

K-Number: K884783 · 1988-11-30

ApplicantAlto Development Corp.
Decision Date1988-11-30
Product CodeFZQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RANEY CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Alto Development Corp.. It received FDA 510(k) clearance on 1988-11-30 under 510(k) number K884783. The device is classified under product code FZQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RANEY CLIP?

RANEY CLIP is a medical device that received FDA 510(k) clearance on 1988-11-30. The listed applicant is Alto Development Corp.. The 510(k) number is K884783.

When did RANEY CLIP receive FDA 510(k) clearance?

RANEY CLIP received FDA 510(k) clearance on 1988-11-30, under 510(k) number K884783.

Who is the listed applicant for RANEY CLIP?

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

What is the FDA product code for RANEY CLIP?

The FDA product code for RANEY CLIP is FZQ.

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 Alto Development 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.

K964621A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTONK932513LABELING FOR MYO/WIRE II STERNOTOMY SUTURESK931537A&E MEDICAL ELECTROSURG ELECTRO W/NON-STICK COATK930528A&E MEDICAL ELECTROSURGICAL CONNECTING CORDSK914193A&E MEDICAL CORP DISPOS SUCT COAG W/NON STICK COATK915300A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES

View all 10 devices →

Related Devices (Code: FZQ)

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.

K873744LEUKOCLIP(R)Beiersdorf, Inc.K830704ONE TIME DISPOSABLE SKIN STAPLERAcme United Corp.K830768DISPOSABLE SKIN STAPLERSurgeons Choice, Inc.K822963SURGICAL PRODUCTS, SKIN STAPLE REMOVERTemp-Stik Corp.K822145COMPLETERichard-Allan Medical Ind., 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.

↑