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FDA 510(k)

PARA 4 PLUS

K-Number: K933844 · 1993-12-27

ApplicantStreck Laboratories, Inc.
Decision Date1993-12-27
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARA 4 PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Streck Laboratories, Inc.. It received FDA 510(k) clearance on 1993-12-27 under 510(k) number K933844. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARA 4 PLUS?

PARA 4 PLUS is a medical device that received FDA 510(k) clearance on 1993-12-27. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K933844.

When did PARA 4 PLUS receive FDA 510(k) clearance?

PARA 4 PLUS received FDA 510(k) clearance on 1993-12-27, under 510(k) number K933844.

Who is the listed applicant for PARA 4 PLUS?

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

What is the FDA product code for PARA 4 PLUS?

The FDA product code for PARA 4 PLUS is JJY.

Other records listing Streck Laboratories, Inc. as applicant

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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.

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