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FDA 510(k)

SURU BLOOD COLLECTION SET

K-Number: K802170 · 1981-04-06

ApplicantSuru Chemicals & Pharmaceuticals, Ltd.
Decision Date1981-04-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURU BLOOD COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Suru Chemicals & Pharmaceuticals, Ltd.. It received FDA 510(k) clearance on 1981-04-06 under 510(k) number K802170. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURU BLOOD COLLECTION SET?

SURU BLOOD COLLECTION SET is a medical device that received FDA 510(k) clearance on 1981-04-06. The listed applicant is Suru Chemicals & Pharmaceuticals, Ltd.. The 510(k) number is K802170.

When did SURU BLOOD COLLECTION SET receive FDA 510(k) clearance?

SURU BLOOD COLLECTION SET received FDA 510(k) clearance on 1981-04-06, under 510(k) number K802170.

Who is the listed applicant for SURU BLOOD COLLECTION SET?

The FDA 510(k) record lists Suru Chemicals & Pharmaceuticals, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURU BLOOD COLLECTION SET?

The FDA product code for SURU BLOOD COLLECTION SET is FPA.

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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 Suru Chemicals & Pharmaceuticals, Ltd. 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.

K811006SOLUTION ADMINISTRATION SETK802169SURU INFUSION SET TYPE JK780658STERILE BLOOD ADMINISTRATION SETK780655STERILE INFUSION SET TYPE SK780657STERILE BLOOD COLLECTION SETK780656STERILE INFUSION SET TYPE J

View all 8 devices →

Related Devices (Code: FPA)

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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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