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FDA 510(k)

MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.

K-Number: K896019 · 1990-01-03

ApplicantDlp, Inc.
Decision Date1990-01-03
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI. is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1990-01-03 under 510(k) number K896019. 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 MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.?

MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI. is a medical device that received FDA 510(k) clearance on 1990-01-03. The listed applicant is Dlp, Inc.. The 510(k) number is K896019.

When did MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI. receive FDA 510(k) clearance?

MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI. received FDA 510(k) clearance on 1990-01-03, under 510(k) number K896019.

Who is the listed applicant for MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.?

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 MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI.?

The FDA product code for MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI. 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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