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FDA 510(k)

VACUUM SUCTION FILTER

K-Number: K812139 · 1981-08-20

ApplicantK & G Healthcare Ind., Inc.
Decision Date1981-08-20
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VACUUM SUCTION FILTER is the device name listed in this FDA 510(k) record. The listed applicant is K & G Healthcare Ind., Inc.. It received FDA 510(k) clearance on 1981-08-20 under 510(k) number K812139. 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 VACUUM SUCTION FILTER?

VACUUM SUCTION FILTER is a medical device that received FDA 510(k) clearance on 1981-08-20. The listed applicant is K & G Healthcare Ind., Inc.. The 510(k) number is K812139.

When did VACUUM SUCTION FILTER receive FDA 510(k) clearance?

VACUUM SUCTION FILTER received FDA 510(k) clearance on 1981-08-20, under 510(k) number K812139.

Who is the listed applicant for VACUUM SUCTION FILTER?

The FDA 510(k) record lists K & G Healthcare Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUUM SUCTION FILTER?

The FDA product code for VACUUM SUCTION FILTER is KDQ.

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 K & G Healthcare Ind., 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.

K812573SPIROMETER FILTERK811546NICHOLAS II, VIRAL-BACTERIAL FILTER

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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