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FDA 510(k)

MODIFIED THORACENTESIS CATHETER

K-Number: K811437 · 1981-08-13

ApplicantBlair Medical Products
Decision Date1981-08-13
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFIED THORACENTESIS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Blair Medical Products. It received FDA 510(k) clearance on 1981-08-13 under 510(k) number K811437. 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 MODIFIED THORACENTESIS CATHETER?

MODIFIED THORACENTESIS CATHETER is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Blair Medical Products. The 510(k) number is K811437.

When did MODIFIED THORACENTESIS CATHETER receive FDA 510(k) clearance?

MODIFIED THORACENTESIS CATHETER received FDA 510(k) clearance on 1981-08-13, under 510(k) number K811437.

Who is the listed applicant for MODIFIED THORACENTESIS CATHETER?

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

What is the FDA product code for MODIFIED THORACENTESIS CATHETER?

The FDA product code for MODIFIED THORACENTESIS CATHETER is KDQ.

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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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