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FDA 510(k)

PULSE LAVAGE

K-Number: K854543 · 1986-01-27

ApplicantTava Surgical Instruments
Decision Date1986-01-27
Product CodeFQH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PULSE LAVAGE is the device name listed in this FDA 510(k) record. The listed applicant is Tava Surgical Instruments. It received FDA 510(k) clearance on 1986-01-27 under 510(k) number K854543. The device is classified under product code FQH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSE LAVAGE?

PULSE LAVAGE is a medical device that received FDA 510(k) clearance on 1986-01-27. The listed applicant is Tava Surgical Instruments. The 510(k) number is K854543.

When did PULSE LAVAGE receive FDA 510(k) clearance?

PULSE LAVAGE received FDA 510(k) clearance on 1986-01-27, under 510(k) number K854543.

Who is the listed applicant for PULSE LAVAGE?

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

What is the FDA product code for PULSE LAVAGE?

The FDA product code for PULSE LAVAGE is FQH.

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Other records listing Tava Surgical Instruments 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.

K935367TAVA WIRE-DRIVERK940109TAVA K-WIREK885273MICRO SURGICAL INSTRUMENT SYSTEMK884492MICRO SURGICAL INSTRUMENT SYSTEMK872475SURGICAL BURK863788SAWBLADE

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Related Devices (Code: FQH)

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.

K253996BD Surgiphor™ Antimicrobial Irrigation System (910110)Becton, Dickinson and Company (BD)K253445BD Surgiphor™ 1000 mL Antimicrobial Irrigation System (910120)BdK231023ERBEJET® 2 SystemErbe Elektromedizin GmbHK220759Armis VeriCyn Wound WashArmis Biopharma, Inc.K220964VERSAJET Hydrosurgery System (III)Smith & Nephew Medical LimitedK221504BD Surgiphor™ Antimicrobial Irrigation SystemBd

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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