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FDA 510(k)

MICRO/PETTOR, SMI

K-Number: K770307 · 1977-04-05

ApplicantLederle Laboratories
Decision Date1977-04-05
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICRO/PETTOR, SMI is the device name listed in this FDA 510(k) record. The listed applicant is Lederle Laboratories. It received FDA 510(k) clearance on 1977-04-05 under 510(k) number K770307. 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 MICRO/PETTOR, SMI?

MICRO/PETTOR, SMI is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Lederle Laboratories. The 510(k) number is K770307.

When did MICRO/PETTOR, SMI receive FDA 510(k) clearance?

MICRO/PETTOR, SMI received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770307.

Who is the listed applicant for MICRO/PETTOR, SMI?

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

What is the FDA product code for MICRO/PETTOR, SMI?

The FDA product code for MICRO/PETTOR, SMI is JQW.

Related Clinical Trials

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Other records listing Lederle 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.

K770975ANTI-CONVULSANT DRUG CONTROLK760467ROTATOR, FIXED SPEED

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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