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FDA 510(k)

MUCUS SPECIMEN TRAP

K-Number: K962168 · 1996-07-22

ApplicantSage Products, Inc.
Decision Date1996-07-22
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MUCUS SPECIMEN TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Sage Products, Inc.. It received FDA 510(k) clearance on 1996-07-22 under 510(k) number K962168. 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 MUCUS SPECIMEN TRAP?

MUCUS SPECIMEN TRAP is a medical device that received FDA 510(k) clearance on 1996-07-22. The listed applicant is Sage Products, Inc.. The 510(k) number is K962168.

When did MUCUS SPECIMEN TRAP receive FDA 510(k) clearance?

MUCUS SPECIMEN TRAP received FDA 510(k) clearance on 1996-07-22, under 510(k) number K962168.

Who is the listed applicant for MUCUS SPECIMEN TRAP?

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

What is the FDA product code for MUCUS SPECIMEN TRAP?

The FDA product code for MUCUS SPECIMEN TRAP is KDQ.

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Other records listing Sage Products, 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.

K972705RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTICK980490SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPSK9739112 GALLON ALTERNATE CARE SHARPS CONTAINERK972279SHARPS SHUTTLEK970135NITRILE GLOVESK972302POCKET COUNT OR SAFETCOUNT

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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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