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FDA 510(k)

DISPOSABLE CHIBA-TYPE NEEDLE

K-Number: K813368 · 1982-01-05

ApplicantDlp, Inc.
Decision Date1982-01-05
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CHIBA-TYPE NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1982-01-05 under 510(k) number K813368. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE CHIBA-TYPE NEEDLE?

DISPOSABLE CHIBA-TYPE NEEDLE is a medical device that received FDA 510(k) clearance on 1982-01-05. The listed applicant is Dlp, Inc.. The 510(k) number is K813368.

When did DISPOSABLE CHIBA-TYPE NEEDLE receive FDA 510(k) clearance?

DISPOSABLE CHIBA-TYPE NEEDLE received FDA 510(k) clearance on 1982-01-05, under 510(k) number K813368.

Who is the listed applicant for DISPOSABLE CHIBA-TYPE NEEDLE?

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

What is the FDA product code for DISPOSABLE CHIBA-TYPE NEEDLE?

The FDA product code for DISPOSABLE CHIBA-TYPE NEEDLE is GAA.

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Other records listing Dlp, 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.

K973485CLEARVIEW BLOWER/MISTERK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)K953945RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLETK950754MACRO SUCTION TUBE MODEL NO 10061K934215CONTAIN-ORK915268CATHETER TWO STAGE VENOUS RETURN

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Related Devices (Code: GAA)

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.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN ACCURA NEEDLEMedical Device Technologies, Inc.

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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