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FDA 510(k)

SHARGHP INSULIN SYRINGES

K-Number: K895980 · 1990-09-07

ApplicantShargh Pharmaceutical Co., Inc.
Decision Date1990-09-07
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARGHP INSULIN SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Shargh Pharmaceutical Co., Inc.. It received FDA 510(k) clearance on 1990-09-07 under 510(k) number K895980. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARGHP INSULIN SYRINGES?

SHARGHP INSULIN SYRINGES is a medical device that received FDA 510(k) clearance on 1990-09-07. The listed applicant is Shargh Pharmaceutical Co., Inc.. The 510(k) number is K895980.

When did SHARGHP INSULIN SYRINGES receive FDA 510(k) clearance?

SHARGHP INSULIN SYRINGES received FDA 510(k) clearance on 1990-09-07, under 510(k) number K895980.

Who is the listed applicant for SHARGHP INSULIN SYRINGES?

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

What is the FDA product code for SHARGHP INSULIN SYRINGES?

The FDA product code for SHARGHP INSULIN SYRINGES is FMF.

Related Clinical Trials

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.

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Other records listing Shargh Pharmaceutical Co., 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.

K013384SHARGHP A.V. FISTULA NEEDLE SETK895810SHARGHP SYRINGES, WITH AND WITHOUT NEEDLEK895812SHARGHP INTRAVENOUS CATHETERK895811SHARGHP HYPODERMIC NEEDLE

Related Devices (Code: FMF)

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.

K262581GraftGun Universal Graft Delivery System (GDS®)SurGenTec, LLCK252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLCK253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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