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FDA 510(k)

SPECTROPHOTOMETEO IL MODEL 651

K-Number: K771604 · 1977-09-22

Decision Date1977-09-22
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETEO IL MODEL 651 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1977-09-22 under 510(k) number K771604. The device is classified under product code JXR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTROPHOTOMETEO IL MODEL 651?

SPECTROPHOTOMETEO IL MODEL 651 is a medical device that received FDA 510(k) clearance on 1977-09-22. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K771604.

When did SPECTROPHOTOMETEO IL MODEL 651 receive FDA 510(k) clearance?

SPECTROPHOTOMETEO IL MODEL 651 received FDA 510(k) clearance on 1977-09-22, under 510(k) number K771604.

Who is the listed applicant for SPECTROPHOTOMETEO IL MODEL 651?

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

What is the FDA product code for SPECTROPHOTOMETEO IL MODEL 651?

The FDA product code for SPECTROPHOTOMETEO IL MODEL 651 is JXR.

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 Instrumentation Laboratory CO 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 315 devices →

Related Devices (Code: JXR)

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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