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FDA 510(k)

CUATICO MYELOGRAPHY NEEDLES

K-Number: K813367 · 1982-01-05

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

Device Summary

CUATICO MYELOGRAPHY NEEDLES 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 K813367. 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 CUATICO MYELOGRAPHY NEEDLES?

CUATICO MYELOGRAPHY NEEDLES 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 K813367.

When did CUATICO MYELOGRAPHY NEEDLES receive FDA 510(k) clearance?

CUATICO MYELOGRAPHY NEEDLES received FDA 510(k) clearance on 1982-01-05, under 510(k) number K813367.

Who is the listed applicant for CUATICO MYELOGRAPHY NEEDLES?

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 CUATICO MYELOGRAPHY NEEDLES?

The FDA product code for CUATICO MYELOGRAPHY NEEDLES is GAA.

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Other records listing Dlp, Inc. as applicant

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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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