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FDA 510(k)

FALLOPIAN TUBE FORCEPS

K-Number: K810483 · 1981-03-11

ApplicantAmerican V. Mueller
Decision Date1981-03-11
Product CodeKNA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FALLOPIAN TUBE FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810483. 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 FALLOPIAN TUBE FORCEPS?

FALLOPIAN TUBE FORCEPS is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is American V. Mueller. The 510(k) number is K810483.

When did FALLOPIAN TUBE FORCEPS receive FDA 510(k) clearance?

FALLOPIAN TUBE FORCEPS received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810483.

Who is the listed applicant for FALLOPIAN TUBE FORCEPS?

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

What is the FDA product code for FALLOPIAN TUBE FORCEPS?

The FDA product code for FALLOPIAN TUBE FORCEPS is KNA.

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Other records listing American V. Mueller 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.

K873771HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTROK873332MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEMK871685HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYSK864676HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEMK862772V. MUELLER (R) GOOSENECK CIRCULAR STAPLERK861471V. MUELLER VITAL CLIP-HEMOSTATIC CLIP

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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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