Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER

K-Number: K850709 · 1985-03-12

Decision Date1985-03-12
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 1985-03-12 under 510(k) number K850709. 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 SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER?

SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1985-03-12. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K850709.

When did SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER receive FDA 510(k) clearance?

SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER received FDA 510(k) clearance on 1985-03-12, under 510(k) number K850709.

Who is the listed applicant for SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER?

The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER?

The FDA product code for SPECTRONIC 501 & 601 - CLINICAL SPECTROPHOTOMETER 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 Bausch & Lomb, 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 92 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑