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FDA 510(k)

DISPENSER ASPIRATOR DA 300

K-Number: K812782 · 1981-10-23

ApplicantPharmacia, Inc.
Decision Date1981-10-23
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DISPENSER ASPIRATOR DA 300 is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1981-10-23 under 510(k) number K812782. 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 DISPENSER ASPIRATOR DA 300?

DISPENSER ASPIRATOR DA 300 is a medical device that received FDA 510(k) clearance on 1981-10-23. The listed applicant is Pharmacia, Inc.. The 510(k) number is K812782.

When did DISPENSER ASPIRATOR DA 300 receive FDA 510(k) clearance?

DISPENSER ASPIRATOR DA 300 received FDA 510(k) clearance on 1981-10-23, under 510(k) number K812782.

Who is the listed applicant for DISPENSER ASPIRATOR DA 300?

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

What is the FDA product code for DISPENSER ASPIRATOR DA 300?

The FDA product code for DISPENSER ASPIRATOR DA 300 is JQW.

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Other records listing Pharmacia, 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.

K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP 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

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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