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FDA 510(k)

BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO

K-Number: K844369 · 1985-01-04

ApplicantPrecision Dynamics Corp.
Decision Date1985-01-04
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO is the device name listed in this FDA 510(k) record. The listed applicant is Precision Dynamics Corp.. It received FDA 510(k) clearance on 1985-01-04 under 510(k) number K844369. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO?

BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO is a medical device that received FDA 510(k) clearance on 1985-01-04. The listed applicant is Precision Dynamics Corp.. The 510(k) number is K844369.

When did BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO receive FDA 510(k) clearance?

BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO received FDA 510(k) clearance on 1985-01-04, under 510(k) number K844369.

Who is the listed applicant for BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO?

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

What is the FDA product code for BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO?

The FDA product code for BBL PORT-A-CUL 21628 DOUBLE SWAB SULTURE COLLECTIO is JSM.

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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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