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FDA 510(k)

SCEPTORPETTE SYSTEM

K-Number: K883907 · 1988-10-27

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1988-10-27
Product CodeLRG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SCEPTORPETTE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1988-10-27 under 510(k) number K883907. The device is classified under product code LRG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCEPTORPETTE SYSTEM?

SCEPTORPETTE SYSTEM is a medical device that received FDA 510(k) clearance on 1988-10-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K883907.

When did SCEPTORPETTE SYSTEM receive FDA 510(k) clearance?

SCEPTORPETTE SYSTEM received FDA 510(k) clearance on 1988-10-27, under 510(k) number K883907.

Who is the listed applicant for SCEPTORPETTE SYSTEM?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCEPTORPETTE SYSTEM?

The FDA product code for SCEPTORPETTE SYSTEM is LRG.

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Related Devices (Code: LRG)

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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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