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FDA 510(k)

MICRO-FLOW SPECTROPHOTOMETER CL-720

K-Number: K801957 · 1980-09-26

Decision Date1980-09-26
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICRO-FLOW SPECTROPHOTOMETER CL-720 is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Precision Instruments, Inc.. It received FDA 510(k) clearance on 1980-09-26 under 510(k) number K801957. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-FLOW SPECTROPHOTOMETER CL-720?

MICRO-FLOW SPECTROPHOTOMETER CL-720 is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Shimadzu Precision Instruments, Inc.. The 510(k) number is K801957.

When did MICRO-FLOW SPECTROPHOTOMETER CL-720 receive FDA 510(k) clearance?

MICRO-FLOW SPECTROPHOTOMETER CL-720 received FDA 510(k) clearance on 1980-09-26, under 510(k) number K801957.

Who is the listed applicant for MICRO-FLOW SPECTROPHOTOMETER CL-720?

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

What is the FDA product code for MICRO-FLOW SPECTROPHOTOMETER CL-720?

The FDA product code for MICRO-FLOW SPECTROPHOTOMETER CL-720 is JJQ.

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.

Other records listing Shimadzu Precision Instruments, 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.

View all 23 devices →

Related Devices (Code: JJQ)

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.

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.

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