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FDA 510(k)

INTRAUTERINE DEVICE REMOVER

K-Number: K842295 · 1984-10-12

ApplicantPremier Dental Products Co.
Decision Date1984-10-12
Product CodeHHF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INTRAUTERINE DEVICE REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Products Co.. It received FDA 510(k) clearance on 1984-10-12 under 510(k) number K842295. The device is classified under product code HHF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAUTERINE DEVICE REMOVER?

INTRAUTERINE DEVICE REMOVER is a medical device that received FDA 510(k) clearance on 1984-10-12. The listed applicant is Premier Dental Products Co.. The 510(k) number is K842295.

When did INTRAUTERINE DEVICE REMOVER receive FDA 510(k) clearance?

INTRAUTERINE DEVICE REMOVER received FDA 510(k) clearance on 1984-10-12, under 510(k) number K842295.

Who is the listed applicant for INTRAUTERINE DEVICE REMOVER?

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

What is the FDA product code for INTRAUTERINE DEVICE REMOVER?

The FDA product code for INTRAUTERINE DEVICE REMOVER is HHF.

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Other records listing Premier Dental Products Co. 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.

K132526KNIT-PAK+K131212PREMIER CERAMIC PRIMERK083695TRAXODENTK062166ENAMEL PROK062683ENAMEL PRO VARNISHK061998PREMIER SELF-ETCHING BOND ENHANCER

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Related Devices (Code: HHF)

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.

K926541IUD HOOKSThomasville Medical Assoc.K891030IUD HOOKS - SIMPLE, UNIVERSAL AND SKLARZinnanti Surgical Instruments, Inc.K831568RELIANCE TEMPO OPHTH. INSTR STANDF. & F. KoenigkramerK820115EMMETT IUD THREAD RETREIVERProto-Med, Inc.K811761THE EMMETT IUD THREAD RETRIEVERProto-Med, 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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