FDA 510(k)

DSD

K-Number: K812983 · 1981-11-10

Decision Date1981-11-10

Product CodeJQW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DSD is the device name listed in this FDA 510(k) record. The listed applicant is Pm America, Inc.. It received FDA 510(k) clearance on 1981-11-10 under 510(k) number K812983. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSD?

DSD is a medical device that received FDA 510(k) clearance on 1981-11-10. The listed applicant is Pm America, Inc.. The 510(k) number is K812983.

When did DSD receive FDA 510(k) clearance?

DSD received FDA 510(k) clearance on 1981-11-10, under 510(k) number K812983.

Who is the listed applicant for DSD?

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

What is the FDA product code for DSD?

The FDA product code for DSD is JQW.

Other records listing Pm America, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K830319AUTO PREP K820748POLI-MAK MODEL F-4 (FINAL K813102POLI-MAK II K801271MODEL 4900 OFF-LINE PREPARATION SYSTEM

Related Devices (Code: JQW)

K023955BD VIPER INSTRUMENTBecton, Dickinson & CO K973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters Corporation K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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.