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FDA 510(k)

SPECTRONIC 2000 SPECTROPHOTOMETER

K-Number: K850767 · 1985-03-14

ApplicantBausch & Lomb, Inc.
Decision Date1985-03-14
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTRONIC 2000 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 1985-03-14 under 510(k) number K850767. 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 2000 SPECTROPHOTOMETER?

SPECTRONIC 2000 SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1985-03-14. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K850767.

When did SPECTRONIC 2000 SPECTROPHOTOMETER receive FDA 510(k) clearance?

SPECTRONIC 2000 SPECTROPHOTOMETER received FDA 510(k) clearance on 1985-03-14, under 510(k) number K850767.

Who is the listed applicant for SPECTRONIC 2000 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 2000 SPECTROPHOTOMETER?

The FDA product code for SPECTRONIC 2000 SPECTROPHOTOMETER is JJQ.

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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.

K192005Bausch + Lomb PreVue Inserter for enVista PreloadedK173480Crystalsert Lens Delivery SystemK161012Easy-Load Lens Delivery SystemK131208BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS FOR PRESBYOPIA,K122575BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS, BAUSCH & LOMB PUREVISION TORIC (BALAFILCON A) VIK113852BAUSCH & LOMB IOL INJECTOR

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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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, Inc.

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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