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FDA 510(k)

SC-360 SPECTROPHOTOMETER

K-Number: K852047 · 1985-05-31

ApplicantPharmacia, Inc.
Decision Date1985-05-31
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SC-360 SPECTROPHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacia, Inc.. It received FDA 510(k) clearance on 1985-05-31 under 510(k) number K852047. 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 SC-360 SPECTROPHOTOMETER?

SC-360 SPECTROPHOTOMETER is a medical device that received FDA 510(k) clearance on 1985-05-31. The listed applicant is Pharmacia, Inc.. The 510(k) number is K852047.

When did SC-360 SPECTROPHOTOMETER receive FDA 510(k) clearance?

SC-360 SPECTROPHOTOMETER received FDA 510(k) clearance on 1985-05-31, under 510(k) number K852047.

Who is the listed applicant for SC-360 SPECTROPHOTOMETER?

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

What is the FDA product code for SC-360 SPECTROPHOTOMETER?

The FDA product code for SC-360 SPECTROPHOTOMETER is JJQ.

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Other records listing Pharmacia, 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.

K974350ALLERGAN IMMUNO CAP M4, M8, K70K972364UNICAP PHADIATOPK972068UNICAP SPECIFIC IGE FEIA ASSAY, LATEX ALLERGEN IMMUNOCAP K82K970420MASTERCAP AM 5.0/MASTERCAP RM 5.0K964152UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMHK962274UNICAP 100

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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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