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FDA 510(k)

SPECTROPHOTOMETER (JUNIOR III)

K-Number: K760112 · 1976-07-16

ApplicantThe Perkin-Elmer Corp.
Decision Date1976-07-16
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETER (JUNIOR III) is the device name listed in this FDA 510(k) record. The listed applicant is The Perkin-Elmer Corp.. It received FDA 510(k) clearance on 1976-07-16 under 510(k) number K760112. 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 SPECTROPHOTOMETER (JUNIOR III)?

SPECTROPHOTOMETER (JUNIOR III) is a medical device that received FDA 510(k) clearance on 1976-07-16. The listed applicant is The Perkin-Elmer Corp.. The 510(k) number is K760112.

When did SPECTROPHOTOMETER (JUNIOR III) receive FDA 510(k) clearance?

SPECTROPHOTOMETER (JUNIOR III) received FDA 510(k) clearance on 1976-07-16, under 510(k) number K760112.

Who is the listed applicant for SPECTROPHOTOMETER (JUNIOR III)?

The FDA 510(k) record lists The Perkin-Elmer Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECTROPHOTOMETER (JUNIOR III)?

The FDA product code for SPECTROPHOTOMETER (JUNIOR III) is JJQ.

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Other records listing The Perkin-Elmer Corp. 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.

K935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPK900828PERKIN-ELMER AA 3100 ATOMIC ABSORPTION SPECTRO.K884864PLASMA 40 INDUCT. COUPLED PLASMA EMMISSION SPECTROK884886MODEL 250 LIQUID CHROMOTAGRAPHY PUMPK872737PERKIN-ELMER LC235 DIODE ARRAY DETECTORK872464ION TRAP DETECTOR (ITD)

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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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