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FDA 510(k)

SUCTION COLLECTION BOTTLE, DISPOSABLE

K-Number: K810574 · 1981-04-21

ApplicantHarvard Laboratories
Decision Date1981-04-21
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUCTION COLLECTION BOTTLE, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Harvard Laboratories. It received FDA 510(k) clearance on 1981-04-21 under 510(k) number K810574. 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 SUCTION COLLECTION BOTTLE, DISPOSABLE?

SUCTION COLLECTION BOTTLE, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1981-04-21. The listed applicant is Harvard Laboratories. The 510(k) number is K810574.

When did SUCTION COLLECTION BOTTLE, DISPOSABLE receive FDA 510(k) clearance?

SUCTION COLLECTION BOTTLE, DISPOSABLE received FDA 510(k) clearance on 1981-04-21, under 510(k) number K810574.

Who is the listed applicant for SUCTION COLLECTION BOTTLE, DISPOSABLE?

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

What is the FDA product code for SUCTION COLLECTION BOTTLE, DISPOSABLE?

The FDA product code for SUCTION COLLECTION BOTTLE, DISPOSABLE is KDQ.

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Other records listing Harvard Laboratories 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.

K822765SIGMOIDOSCOPE, FLEXIBLEK810573TUBE FEEDING SETK800877ANESTHESIA EXTENSION TUBESK800878SECONDARY I.V. TUBING SETSK800879CLEAR PLASTIC CONNECTING TUBESK800880PLASTIC TUBING ADAPTERS 5-IN-1-

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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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