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FDA 510(k)

MODEL 2650 HIGH CAPACITY DUAL SYRINGE

K-Number: K813644 · 1982-02-18

ApplicantHarvard Apparatus, Inc.
Decision Date1982-02-18
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 2650 HIGH CAPACITY DUAL SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Harvard Apparatus, Inc.. It received FDA 510(k) clearance on 1982-02-18 under 510(k) number K813644. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2650 HIGH CAPACITY DUAL SYRINGE?

MODEL 2650 HIGH CAPACITY DUAL SYRINGE is a medical device that received FDA 510(k) clearance on 1982-02-18. The listed applicant is Harvard Apparatus, Inc.. The 510(k) number is K813644.

When did MODEL 2650 HIGH CAPACITY DUAL SYRINGE receive FDA 510(k) clearance?

MODEL 2650 HIGH CAPACITY DUAL SYRINGE received FDA 510(k) clearance on 1982-02-18, under 510(k) number K813644.

Who is the listed applicant for MODEL 2650 HIGH CAPACITY DUAL SYRINGE?

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

What is the FDA product code for MODEL 2650 HIGH CAPACITY DUAL SYRINGE?

The FDA product code for MODEL 2650 HIGH CAPACITY DUAL SYRINGE is FRN.

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Other records listing Harvard Apparatus, Inc. as applicant

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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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