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FDA 510(k)

CARAWAY TUBES, HEPARIN AND PLAIN

K-Number: K881262 · 1988-05-06

ApplicantHelps Products, Inc.
Decision Date1988-05-06
Product CodeGIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CARAWAY TUBES, HEPARIN AND PLAIN is the device name listed in this FDA 510(k) record. The listed applicant is Helps Products, Inc.. It received FDA 510(k) clearance on 1988-05-06 under 510(k) number K881262. The device is classified under product code GIO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAWAY TUBES, HEPARIN AND PLAIN?

CARAWAY TUBES, HEPARIN AND PLAIN is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Helps Products, Inc.. The 510(k) number is K881262.

When did CARAWAY TUBES, HEPARIN AND PLAIN receive FDA 510(k) clearance?

CARAWAY TUBES, HEPARIN AND PLAIN received FDA 510(k) clearance on 1988-05-06, under 510(k) number K881262.

Who is the listed applicant for CARAWAY TUBES, HEPARIN AND PLAIN?

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

What is the FDA product code for CARAWAY TUBES, HEPARIN AND PLAIN?

The FDA product code for CARAWAY TUBES, HEPARIN AND PLAIN is GIO.

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 Helps Products, 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.

K881188BLOOD PH CAPILLARY TUBES, HEPARINK881186MICROHEMATOCRIT TUBES, HEPARIN & MICROHEMA TUBE,PLK881187NATELSON TUBES, HEPARIN AND PLAIN

Related Devices (Code: GIO)

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.

K972969QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEMInnovative Medical Technologies, Inc.K941291MONOJECT SAMPLETTE SEPARATOR TUBESherwood Medical Co.K894851TRU-TRAXHumagen, Inc.K885324HEMA(PRO)TEC(TION)Medical Products Search, Inc.K885138CAPILLARY TUBE, BLOOD COLLECTIONCoeur Laboratories, Inc.K884623SAFE-TEC CAPILLARY BLOOD COLLECTION TUBESafe-Tec Clinical Products, 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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