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FDA 510(k)

ASTRA DISPOSABLE SPRAY CANNULA

K-Number: K894755 · 1990-01-12

ApplicantAstra Pharmaceutical Products, Inc.
Decision Date1990-01-12
Product CodeCCT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ASTRA DISPOSABLE SPRAY CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Astra Pharmaceutical Products, Inc.. It received FDA 510(k) clearance on 1990-01-12 under 510(k) number K894755. The device is classified under product code CCT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASTRA DISPOSABLE SPRAY CANNULA?

ASTRA DISPOSABLE SPRAY CANNULA is a medical device that received FDA 510(k) clearance on 1990-01-12. The listed applicant is Astra Pharmaceutical Products, Inc.. The 510(k) number is K894755.

When did ASTRA DISPOSABLE SPRAY CANNULA receive FDA 510(k) clearance?

ASTRA DISPOSABLE SPRAY CANNULA received FDA 510(k) clearance on 1990-01-12, under 510(k) number K894755.

Who is the listed applicant for ASTRA DISPOSABLE SPRAY CANNULA?

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

What is the FDA product code for ASTRA DISPOSABLE SPRAY CANNULA?

The FDA product code for ASTRA DISPOSABLE SPRAY CANNULA is CCT.

Related Clinical Trials

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.

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Other records listing Astra Pharmaceutical Products, 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.

K851903ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN

Related Devices (Code: CCT)

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.

K240114UltraEzAir® (UEA1A)Dualams, Inc., Dba AirkorK172956Medicant Mucosal AtomizerMedica Holdings, LLCK153470MADgic Laryngo-Tracheal Mucosal Atomization DeviceTeleflex MedicalK093584EZ-MISTERN.M. Beale Co., Inc.K070596TOPICAL APPLICATORSharn, Inc.K002255LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE (MADGIC)Wolfe Tory Medical, Inc.

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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