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FDA 510(k)

MICROINFERTILITY FORCEPS, TITANIUM

K-Number: K844823 · 1985-01-16

ApplicantPrecision Surgical Instrument, Inc.
Decision Date1985-01-16
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MICROINFERTILITY FORCEPS, TITANIUM is the device name listed in this FDA 510(k) record. The listed applicant is Precision Surgical Instrument, Inc.. It received FDA 510(k) clearance on 1985-01-16 under 510(k) number K844823. The device is classified under product code KNA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROINFERTILITY FORCEPS, TITANIUM?

MICROINFERTILITY FORCEPS, TITANIUM is a medical device that received FDA 510(k) clearance on 1985-01-16. The listed applicant is Precision Surgical Instrument, Inc.. The 510(k) number is K844823.

When did MICROINFERTILITY FORCEPS, TITANIUM receive FDA 510(k) clearance?

MICROINFERTILITY FORCEPS, TITANIUM received FDA 510(k) clearance on 1985-01-16, under 510(k) number K844823.

Who is the listed applicant for MICROINFERTILITY FORCEPS, TITANIUM?

The FDA 510(k) record lists Precision Surgical Instrument, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROINFERTILITY FORCEPS, TITANIUM?

The FDA product code for MICROINFERTILITY FORCEPS, TITANIUM is KNA.

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.

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Other records listing Precision Surgical Instrument, Inc. 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.

K844821MICROINFERTILITY NEEDLE HOLDER, TITANIUMK844822MICROINFERTILITY SCISSORS, TITANIUM

Related Devices (Code: KNA)

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.

K102141COOK WORD BARTHOLIN GLAND CATHETER (FINAL TRADE NAME NOT YET DETERMINED)Cook Urological, Inc.K093904GLENVEIGH VAGINAL TAMPONADE BALLOON CATHETERGlenveigh Surgical, LLCK082939COOK FETAL MEMBRANE MANIPULATOR, MODEL -FMM-122400Cook Urological, Inc.K062438BAKRI POSTPARTUM BALLOON, MODEL J-SOS-100500Cook Ob/GynK060289EPISTAT, V-STAT, MODELS EPISTAT-001-01, V-STAT-001-01Frontline MedicalK013597TAMPONADE UTERINE BALLOON CATHETER SETCook Ob/Gyn

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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