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FDA 510(k)

PRECEPT CEFTAZIDIME

K-Number: K862446 · 1986-07-11

ApplicantAustin Biological Laboratories
Decision Date1986-07-11
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PRECEPT CEFTAZIDIME is the device name listed in this FDA 510(k) record. The listed applicant is Austin Biological Laboratories. It received FDA 510(k) clearance on 1986-07-11 under 510(k) number K862446. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECEPT CEFTAZIDIME?

PRECEPT CEFTAZIDIME is a medical device that received FDA 510(k) clearance on 1986-07-11. The listed applicant is Austin Biological Laboratories. The 510(k) number is K862446.

When did PRECEPT CEFTAZIDIME receive FDA 510(k) clearance?

PRECEPT CEFTAZIDIME received FDA 510(k) clearance on 1986-07-11, under 510(k) number K862446.

Who is the listed applicant for PRECEPT CEFTAZIDIME?

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

What is the FDA product code for PRECEPT CEFTAZIDIME?

The FDA product code for PRECEPT CEFTAZIDIME is JWY.

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Other records listing Austin Biological Laboratories 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.

K880511XACT NEISSERIAK874727PRECEPT(TM) CIPROFLOXACINK870769AUSTIN NONFERMENTER KITK864069PRECEPT (TM) TICARCILLIN/CLAVULANIC ACIDK862560PRECEPT CEFTIZOXIMEK860195PRECEPT TRIMETHOPRIM/SULFAMETHOXAZOLE

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Related Devices (Code: JWY)

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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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