FDA 510(k)

SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN

K-Number: K882911 · 1988-08-17

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1988-08-17

Product CodeJWY

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN 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 1988-08-17 under 510(k) number K882911. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN?

SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN is a medical device that received FDA 510(k) clearance on 1988-08-17. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K882911.

When did SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN receive FDA 510(k) clearance?

SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN received FDA 510(k) clearance on 1988-08-17, under 510(k) number K882911.

Who is the listed applicant for SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN?

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 SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN?

The FDA product code for SCEPTOR EXTEN. OF CONCENTRATION RANGE: PENCILLIN is JWY.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.