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FDA 510(k)

TOP STERILE DISPOS. HYPODERMIC NEEDLES

K-Number: K832626 · 1983-10-14

ApplicantTop Surgical Manufacturers Co.
Decision Date1983-10-14
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TOP STERILE DISPOS. HYPODERMIC NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Top Surgical Manufacturers Co.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832626. 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 TOP STERILE DISPOS. HYPODERMIC NEEDLES?

TOP STERILE DISPOS. HYPODERMIC NEEDLES is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Top Surgical Manufacturers Co.. The 510(k) number is K832626.

When did TOP STERILE DISPOS. HYPODERMIC NEEDLES receive FDA 510(k) clearance?

TOP STERILE DISPOS. HYPODERMIC NEEDLES received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832626.

Who is the listed applicant for TOP STERILE DISPOS. HYPODERMIC NEEDLES?

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

What is the FDA product code for TOP STERILE DISPOS. HYPODERMIC NEEDLES?

The FDA product code for TOP STERILE DISPOS. HYPODERMIC NEEDLES is GAA.

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Other records listing Top Surgical Manufacturers Co. 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.

K844343TOP SINGLE USE U.T.W. A-V FISTULA NEEDLE Y TYPEK843415TOP HYPODERMIC SYRINGE LUER LOCKK843313TOP DISPOSABLE SPINAL NEEDLEK843414TOP HYPODERMIC SYRINGE PISTONK841119TOPS DISPOS. INFUSION SET/HEMODIALYSISK841025TOP DISPOSABLE INFUSION SET

View all 12 devices →

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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