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FDA 510(k)

SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000

K-Number: K872749 · 1987-09-16

ApplicantSecomam Co.
Decision Date1987-09-16
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Secomam Co.. It received FDA 510(k) clearance on 1987-09-16 under 510(k) number K872749. 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 SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000?

SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000 is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Secomam Co.. The 510(k) number is K872749.

When did SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000 receive FDA 510(k) clearance?

SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000 received FDA 510(k) clearance on 1987-09-16, under 510(k) number K872749.

Who is the listed applicant for SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000?

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

What is the FDA product code for SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000?

The FDA product code for SPECTROPHOTOMETERS MODELS:ABC+,ABC,S 500, S 1000 is JJQ.

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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

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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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