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FDA 510(k)

FEMORAL CANAL SUCTION TAMPON

K-Number: K831999 · 1983-09-29

ApplicantRichards Manufacturer Co.
Decision Date1983-09-29
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FEMORAL CANAL SUCTION TAMPON is the device name listed in this FDA 510(k) record. The listed applicant is Richards Manufacturer Co.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K831999. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FEMORAL CANAL SUCTION TAMPON?

FEMORAL CANAL SUCTION TAMPON is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Richards Manufacturer Co.. The 510(k) number is K831999.

When did FEMORAL CANAL SUCTION TAMPON receive FDA 510(k) clearance?

FEMORAL CANAL SUCTION TAMPON received FDA 510(k) clearance on 1983-09-29, under 510(k) number K831999.

Who is the listed applicant for FEMORAL CANAL SUCTION TAMPON?

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

What is the FDA product code for FEMORAL CANAL SUCTION TAMPON?

The FDA product code for FEMORAL CANAL SUCTION TAMPON is JOL.

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 Richards Manufacturer 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.

K831884SPECTRON EXTRA-SMALL, STRAIGHT FEMORALK832000THIGH HOLDERK831656ARTHROSCOPY KNIVES/PROBES/BENDING TOOL

Related Devices (Code: JOL)

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.

K051370STERILE SALINE FOR DEVICE CARE, STERILE WATER FOR DEVICE CARE, MODELS 2F7121, 2F8014Baxter Healthcare CorpK000266PRIMARY CARE SOLUTIONS STERILE SALINE-0.9% SODIUM CHLORIDE FOR DEVICE IRRIGATIONPrimary Care Solutions, Inc.K000265PRIMARY CARE SOLUTIONS STERILE WATER DEVICE IRRIGATIONPrimary Care Solutions, Inc.K003402WELCON STERILE WATER FOR DEVICE IRRIGATION; WELCON STERILE 0.9% NORMAL SALINE FOR DEVICE IRRIGATIONWelcon, Inc.K994321STERILE WATER AND 0.9% SODIUM CHLORIDE FOR IRRIGATION, USPAutomatic Liquid Packaging, Inc.K974758HYDROX STERILE WATER 4 OZ. CUP 120 ML., HYDROX STERILE WATER 100 ML BOTTLEHydrox Laboratories

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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