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FDA 510(k)

FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL

K-Number: K884514 · 1988-11-17

ApplicantGatewood and Associates, Ltd.
Decision Date1988-11-17
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL is the device name listed in this FDA 510(k) record. The listed applicant is Gatewood and Associates, Ltd.. It received FDA 510(k) clearance on 1988-11-17 under 510(k) number K884514. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL?

FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL is a medical device that received FDA 510(k) clearance on 1988-11-17. The listed applicant is Gatewood and Associates, Ltd.. The 510(k) number is K884514.

When did FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL receive FDA 510(k) clearance?

FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL received FDA 510(k) clearance on 1988-11-17, under 510(k) number K884514.

Who is the listed applicant for FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL?

The FDA 510(k) record lists Gatewood and Associates, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL?

The FDA product code for FORCEPS, TOWEL, BACKHAUS-TSK (BRAND) TOWEL is GEN.

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 Gatewood and Associates, Ltd. 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.

K884515BONE FILE, SELDIN, #11-TSK BONE FILE, DOUBLE-ENDED

Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, 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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