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FDA 510(k)

TAGG DISPOSABLE VAGINAL SPECULUM

K-Number: K021849 · 2002-07-16

ApplicantTagg Industries
Decision Date2002-07-16
Product CodeHIB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAGG DISPOSABLE VAGINAL SPECULUM is the device name listed in this FDA 510(k) record. The listed applicant is Tagg Industries. It received FDA 510(k) clearance on 2002-07-16 under 510(k) number K021849. The device is classified under product code HIB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAGG DISPOSABLE VAGINAL SPECULUM?

TAGG DISPOSABLE VAGINAL SPECULUM is a medical device that received FDA 510(k) clearance on 2002-07-16. The listed applicant is Tagg Industries. The 510(k) number is K021849.

When did TAGG DISPOSABLE VAGINAL SPECULUM receive FDA 510(k) clearance?

TAGG DISPOSABLE VAGINAL SPECULUM received FDA 510(k) clearance on 2002-07-16, under 510(k) number K021849.

Who is the listed applicant for TAGG DISPOSABLE VAGINAL SPECULUM?

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

What is the FDA product code for TAGG DISPOSABLE VAGINAL SPECULUM?

The FDA product code for TAGG DISPOSABLE VAGINAL SPECULUM is HIB.

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 Tagg Industries 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.

K9462253M FILTRETE(TM) AIR FILTER MEDIAK864472PERSON TO PERSON VALVE-MASK & TRI-SEAL FACE MASK

Related Devices (Code: HIB)

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.

K252208JFord Speculum Sleeve™Ford Medtech, LLCK130046CLEARSPEC SINGLE USE VAGINAL SPECULUMClearspec, LLCK120743SPECULUM, VAGINAL, NONMETALWelch Allyn, Inc.K110766KOLPLUX SYSTEMKolplast CI LtdaK092870NON-STERILE DISPOSABLE VAGINAL SPECULUMKunshan Deyi Plastic Co., Ltd.K091937OFFICE-SPEC DISPOSABLE SIDE-OPENING SPECULUMObp Corporation

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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