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FDA 510(k)

PM9000 VAC TRAP

K-Number: K941818 · 1994-12-12

ApplicantPrecision Medical, Inc.
Decision Date1994-12-12
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PM9000 VAC TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical, Inc.. It received FDA 510(k) clearance on 1994-12-12 under 510(k) number K941818. 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 PM9000 VAC TRAP?

PM9000 VAC TRAP is a medical device that received FDA 510(k) clearance on 1994-12-12. The listed applicant is Precision Medical, Inc.. The 510(k) number is K941818.

When did PM9000 VAC TRAP receive FDA 510(k) clearance?

PM9000 VAC TRAP received FDA 510(k) clearance on 1994-12-12, under 510(k) number K941818.

Who is the listed applicant for PM9000 VAC TRAP?

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

What is the FDA product code for PM9000 VAC TRAP?

The FDA product code for PM9000 VAC TRAP 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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