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FDA 510(k)

SCC-23 SAFETY CLAMP AND CUTTER

K-Number: K982464 · 1998-08-11

ApplicantWomen First Healthcare, Inc.
Decision Date1998-08-11
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SCC-23 SAFETY CLAMP AND CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Women First Healthcare, Inc.. It received FDA 510(k) clearance on 1998-08-11 under 510(k) number K982464. 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 SCC-23 SAFETY CLAMP AND CUTTER?

SCC-23 SAFETY CLAMP AND CUTTER is a medical device that received FDA 510(k) clearance on 1998-08-11. The listed applicant is Women First Healthcare, Inc.. The 510(k) number is K982464.

When did SCC-23 SAFETY CLAMP AND CUTTER receive FDA 510(k) clearance?

SCC-23 SAFETY CLAMP AND CUTTER received FDA 510(k) clearance on 1998-08-11, under 510(k) number K982464.

Who is the listed applicant for SCC-23 SAFETY CLAMP AND CUTTER?

The FDA 510(k) record lists Women First Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCC-23 SAFETY CLAMP AND CUTTER?

The FDA product code for SCC-23 SAFETY CLAMP AND CUTTER is KNA.

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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

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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