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FDA 510(k)

SEP-T-VAC SUCTION CANNISTER W/ TUBING

K-Number: K790379 · 1979-04-10

ApplicantSherwood Medical Co.
Decision Date1979-04-10
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SEP-T-VAC SUCTION CANNISTER W/ TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1979-04-10 under 510(k) number K790379. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEP-T-VAC SUCTION CANNISTER W/ TUBING?

SEP-T-VAC SUCTION CANNISTER W/ TUBING is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Sherwood Medical Co.. The 510(k) number is K790379.

When did SEP-T-VAC SUCTION CANNISTER W/ TUBING receive FDA 510(k) clearance?

SEP-T-VAC SUCTION CANNISTER W/ TUBING received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790379.

Who is the listed applicant for SEP-T-VAC SUCTION CANNISTER W/ TUBING?

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

What is the FDA product code for SEP-T-VAC SUCTION CANNISTER W/ TUBING?

The FDA product code for SEP-T-VAC SUCTION CANNISTER W/ TUBING is KDQ.

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Other records listing Sherwood Medical 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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Related Devices (Code: KDQ)

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.

K081718EXPRESS CHEST DRAINAtrium Medical Corp.K062302MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEMMillicore ABK043582OCEAN CHEST DRAINAtrium Medical Corp.K984496ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAINAtrium Medical Corp.K962856PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTRDeknatel, Inc.K961287ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEMRocket Medical Plc

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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