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FDA 510(k)

IN-LINE BURETTE SET

K-Number: K772036 · 1977-11-16

ApplicantAbbott Laboratories
Decision Date1977-11-16
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IN-LINE BURETTE SET is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1977-11-16 under 510(k) number K772036. 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 IN-LINE BURETTE SET?

IN-LINE BURETTE SET is a medical device that received FDA 510(k) clearance on 1977-11-16. The listed applicant is Abbott Laboratories. The 510(k) number is K772036.

When did IN-LINE BURETTE SET receive FDA 510(k) clearance?

IN-LINE BURETTE SET received FDA 510(k) clearance on 1977-11-16, under 510(k) number K772036.

Who is the listed applicant for IN-LINE BURETTE SET?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IN-LINE BURETTE SET?

The FDA product code for IN-LINE BURETTE SET is FPA.

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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.

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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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