FDA 510(k)

SCEPTOR ENTERIC MIC/ID PANEL (REVISED 4/88)

K-Number: K882301 · 1988-07-12

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1988-07-12

Product CodeJWY

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SCEPTOR ENTERIC MIC/ID PANEL (REVISED 4/88) 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 1988-07-12 under 510(k) number K882301. 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 ENTERIC MIC/ID PANEL (REVISED 4/88)?

SCEPTOR ENTERIC MIC/ID PANEL (REVISED 4/88) is a medical device that received FDA 510(k) clearance on 1988-07-12. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K882301.

When did SCEPTOR ENTERIC MIC/ID PANEL (REVISED 4/88) receive FDA 510(k) clearance?

SCEPTOR ENTERIC MIC/ID PANEL (REVISED 4/88) received FDA 510(k) clearance on 1988-07-12, under 510(k) number K882301.

Who is the listed applicant for SCEPTOR ENTERIC MIC/ID PANEL (REVISED 4/88)?

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 ENTERIC MIC/ID PANEL (REVISED 4/88)?

The FDA product code for SCEPTOR ENTERIC MIC/ID PANEL (REVISED 4/88) is JWY.

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Official Source

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