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FDA 510(k)

TERUMO DISPOSABLE SPINAL NEEDLE

K-Number: K760775 · 1976-11-01

ApplicantTerumo America, Inc.
Decision Date1976-11-01
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TERUMO DISPOSABLE SPINAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Terumo America, Inc.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760775. 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 TERUMO DISPOSABLE SPINAL NEEDLE?

TERUMO DISPOSABLE SPINAL NEEDLE is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Terumo America, Inc.. The 510(k) number is K760775.

When did TERUMO DISPOSABLE SPINAL NEEDLE receive FDA 510(k) clearance?

TERUMO DISPOSABLE SPINAL NEEDLE received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760775.

Who is the listed applicant for TERUMO DISPOSABLE SPINAL NEEDLE?

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

What is the FDA product code for TERUMO DISPOSABLE SPINAL NEEDLE?

The FDA product code for TERUMO DISPOSABLE SPINAL NEEDLE is GAA.

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Other records listing Terumo America, 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.

K811523PLASMA FLEXK802970TERUMO HOLLOW FIBER OXYGENATORK802122CLIRANS TH13 HOLLOW FIBER DIALYZERK802441CLIRANS TH10 HOLLOW FIBER DIALYZERK801193CLIRANS TE15 HOLLOW FIBER DIALYZERK801194CLIRANS TE07 HOLLOW FIBER DIALYZER

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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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